MYL2 Gene

HGNC Family	Myosin light chains (MYL), EF-hand domain containing
Name	myosin, light chain 2, regulatory, cardiac, slow
Description	This gene encodes a major sarcomeric protein in mammalian striated muscle. The encoded protein plays a role in embryonic heart muscle structure and function, while phosphorylation of the encoded protein is involved in cardiac myosin cycling kinetics, torsion and function in adults. Mutations in this gene are associated with hypertrophic cardiomyopathy 10 and infant-onset myopathy. [provided by RefSeq, May 2022]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nMYL2 encodes the ventricular myosin regulatory light chain (MLC‐2v), a 19‐kDa EF‐hand calcium-binding sarcomeric protein that is essential for modulating myosin cross-bridge cycling kinetics, calcium‐dependent contraction, and overall cardiac performance. Phosphorylation of MYL2 is a key regulatory mechanism that fine-tunes the rate and force of contraction as well as cardiac torsion, thereby ensuring efficient myocardial function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nGenetic alterations in MYL2 have been widely implicated in diverse cardiomyopathies. Several studies have identified missense mutations (for example, Glu22Lys, Arg58Gln, R58Q, and A13T), frameshift alleles, and point mutations such as D94A that disrupt the binding of MYL2 to the myosin heavy chain, disturb cross-bridge kinetics, and alter calcium sensitivity of contraction. These mutation‐induced changes lead to phenotypes ranging from hypertrophic cardiomyopathy—with either benign or malignant features—to dilated and restrictive cardiomyopathies, and even to a distinct cardioskeletal myopathy. Such molecular defects, which result in abnormal ATPase activity and impaired force generation, have been demonstrated in human patients as well as in transgenic mouse and induced pluripotent stem cell models."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "2", "end_ref": "13"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition to its central role in force generation, MYL2 function is modulated by a variety of post-translational modifications that affect its stability and interaction with other sarcomeric proteins. Oxidative stress and hypoxia–reoxygenation can induce nitration of MLC-2, increasing its susceptibility to degradation, while alterations in glycosylation have been linked to shifts in muscle phenotype under prolonged unloading. Moreover, variants in the genomic region encompassing MYL2 have been associated with metabolic traits such as body mass index, and evolutionary studies underscore its highly conserved role in both cardiac and slow-twitch skeletal muscles. Together, these findings highlight the multifaceted regulation of MYL2—through phosphorylation, nitration, glycosylation, and energetic state transitions—that is critical for maintaining normal cardiac contractility and overall muscle homeostasis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "14", "end_ref": "17"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Farah Sheikh, Robert C Lyon, Ju Chen "}, {"type": "b", "children": [{"type": "t", "text": "Functions of myosin light chain-2 (MYL2) in cardiac muscle and disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gene (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.gene.2015.06.027"}], "href": "https://doi.org/10.1016/j.gene.2015.06.027"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26074085"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26074085"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Zhyldyz T Kabaeva, Andreas Perrot, Bastian Wolter, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Hum Genet (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.ejhg.5200872"}], "href": "https://doi.org/10.1038/sj.ejhg.5200872"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12404107"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12404107"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Daniel Vega Møller, Paal Skytt Andersen, Paula Hedley, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Hum Genet (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ejhg.2009.34"}], "href": "https://doi.org/10.1038/ejhg.2009.34"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19293840"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19293840"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Colleen Caleshu, Rahul Sakhuja, Robert L Nussbaum, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Furthering the link between the sarcomere and primary cardiomyopathies: restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet A (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.a.34097"}], "href": "https://doi.org/10.1002/ajmg.a.34097"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21823217"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21823217"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "W Glenn L Kerrick, Katarzyna Kazmierczak, Yuanyuan Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FASEB J (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1096/fj.08-118182"}], "href": "https://doi.org/10.1096/fj.08-118182"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18987303"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18987303"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Godelieve R F Claes, Florence H J van Tienen, Patrick Lindsey, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur Heart J (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/eurheartj/ehv522"}], "href": "https://doi.org/10.1093/eurheartj/ehv522"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26497160"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26497160"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Marian A J Weterman, Peter G Barth, Karin Y van Spaendonck-Zwarts, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/brain/aws293"}], "href": "https://doi.org/10.1093/brain/aws293"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "23365102"}], "href": "https://pubmed.ncbi.nlm.nih.gov/23365102"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Wenrui Huang, Jingsheng Liang, Chen-Ching Yuan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS J (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/febs.13286"}], "href": "https://doi.org/10.1111/febs.13286"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25825243"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25825243"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Michael Leist, Maia Datunashvilli, Tatyana Kanyshkova, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Myosin regulatory light chain mutation found in hypertrophic cardiomyopathy patients increases isometric force production in transgenic mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem J (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/BJ20111145"}], "href": "https://doi.org/10.1042/BJ20111145"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22091967"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22091967"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Chen-Ching Yuan, Katarzyna Kazmierczak, Jingsheng Liang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Molecular basis of force-pCa relation in "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "MYL2"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": " cardiomyopathy mice: Role of the super-relaxed state of myosin."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Proc Natl Acad Sci U S A (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1073/pnas.2110328119"}], "href": "https://doi.org/10.1073/pnas.2110328119"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35177471"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35177471"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Katarzyna Kazmierczak, Jingsheng Liang, Chen-Ching Yuan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Slow-twitch skeletal muscle defects accompany cardiac dysfunction in transgenic mice with a mutation in the myosin regulatory light chain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FASEB J (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1096/fj.201801402R"}], "href": "https://doi.org/10.1096/fj.201801402R"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30365366"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30365366"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Thomas Kampourakis, Saraswathi Ponnam, Malcolm Irving "}, {"type": "b", "children": [{"type": "t", "text": "Hypertrophic cardiomyopathy mutation R58Q in the myosin regulatory light chain perturbs thick filament-based regulation in cardiac muscle."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Cell Cardiol (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.yjmcc.2018.02.009"}], "href": "https://doi.org/10.1016/j.yjmcc.2018.02.009"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29452157"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29452157"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Wanqing Wen, Wei Zheng, Yukinori Okada, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Neonatal asphyxia induces the nitration of cardiac myosin light chain 2 that is associated with cardiac systolic dysfunction."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Shock (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1097/SHK.0b013e3181e14f1d"}], "href": "https://doi.org/10.1097/SHK.0b013e3181e14f1d"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20386496"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20386496"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Laurence Stevens, Bruno Bastide, Julie Hedou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Potential regulation of human muscle plasticity by MLC2 post-translational modifications during bed rest and countermeasures."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Arch Biochem Biophys (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.abb.2013.10.016"}], "href": "https://doi.org/10.1016/j.abb.2013.10.016"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24184274"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24184274"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Lieke Gerrits, Gijs J Overheul, Ronny C Derks, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Gene duplication and conversion events shaped three homologous, differentially expressed myosin regulatory light chain (MLC2) genes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Cell Biol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ejcb.2012.02.001"}], "href": "https://doi.org/10.1016/j.ejcb.2012.02.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22425609"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22425609"}]}]}]}
Synonyms	CMH10, MLC-2s/v, MLC2
Proteins	MLRV_HUMAN
NCBI Gene ID	4633
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

MYL2 has 8,415 functional associations with biological entities spanning 8 categories (molecular profile, organism, functional term, phrase or reference, chemical, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 131 datasets.

Click the + buttons to view associations for MYL2 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

MYL2 Gene

Functional Associations

Please acknowledge the Harmonizome in your publications by citing the following reference(s):

	Dataset	Summary
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of MYL2 gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles	tissues with high or low expression of MYL2 gene relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles	tissue samples with high or low expression of MYL2 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray	tissue samples with high or low expression of MYL2 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
	Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of MYL2 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	Biocarta Pathways	pathways involving MYL2 protein from the Biocarta Pathways dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of MYL2 gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset.
	BioGPS Human Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of MYL2 gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
	BioGPS Mouse Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of MYL2 gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	Carcinogenome Chemical Perturbation Carcinogenicity Signatures	small molecule perturbations changing expression of MYL2 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of MYL2 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
	CCLE Cell Line Gene Expression Profiles	cell lines with high or low expression of MYL2 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with MYL2 gene from the CellMarker Gene-Cell Type Associations dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of MYL2 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of MYL2 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
	ChEA Transcription Factor Targets 2022	transcription factors binding the promoter of MYL2 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations	phenotypes associated with MYL2 gene from the curated ClinVar Gene-Phenotype Associations dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with MYL2 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	CM4AI KOLF21J CRISPRi Gene Perturbation Atlas	gene perturbations changing expression of MYL2 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of MYL2 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing MYL2 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing MYL2 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with MYL2 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025	cellular components co-occuring with MYL2 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of MYL2 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with MYL2 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with MYL2 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with MYL2 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by MYL2 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DGIdb Drug Targets 2026	interacting drugs for MYL2 protein from the DGIdb Drug Targets 2026 dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores	diseases involving MYL2 gene from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores 2025	diseases involving MYL2 gene from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores	diseases associated with MYL2 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with MYL2 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with MYL2 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores 2025	diseases co-occuring with MYL2 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
	DisGeNET Gene-Disease Associations	diseases associated with MYL2 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with MYL2 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at MYL2 gene from the ENCODE Histone Modification Site Profiles dataset.
	ENCODE Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of MYL2 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.