EnhancerDB
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  3. rs766656[chr19:5536761]
Enhancers that have rs766656[chr19:5536761]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr19 5534301 5542184 enh44623
Skin (Keratinocyte) Prostate (RWPE1) Lung Stomach Pancreas Muscle (Myotube) Heart
chr19 5536566 5536826 vista28395
VISTA
Transcript factors that have rs766656[chr19:5536761]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr19 5535887 5536932 ZNF274 GTRD no Bone Marrow (K562) 108375266
chr19 5535949 5537099 TCF7L2 GTRD no Colon (HCT116) 108375267
chr19 5536042 5537005 TCF7L2 GTRD no Colon (HCT116) 108375268
chr19 5536044 5537265 TCF7L2 GTRD no Colon (HCT116) 108375269
chr19 5536068 5537086 TCF7L2 GTRD no Colon (HCT116) 108375270
chr19 5536075 5537119 TCF7L2 GTRD no Colon (HCT116) 108375271
chr19 5536161 5536831 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108375272
chr19 5536171 5536930 ZNF274 GTRD no Bone Marrow (K562) 108375273
chr19 5536211 5537057 TCF7L2 GTRD no Colon (HCT116) 108375274
chr19 5536223 5536827 ZNF274 GTRD no Bone Marrow (K562) 108375275
chr19 5536238 5536827 ZNF263 UCSC Txn Factor no Conserved 108375276
chr19 5536242 5537102 ZNF274 GTRD no Bone Marrow (K562) 108375277
chr19 5536260 5536926 TCF7L2 GTRD no Colon (HCT116) 108375278
chr19 5536387 5536821 ZNF274 GTRD no Bone Marrow (K562) 108375279
chr19 5536389 5536799 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108375280
chr19 5536436 5536973 SOX2 GTRD no Neural Stem Cells (H9) 108375281
chr19 5536448 5536772 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108375282
chr19 5536453 5536763 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108375283
chr19 5536453 5536789 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108375284
chr19 5536459 5536835 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108375285
chr19 5536480 5536821 ZNF274 GTRD no Bone Marrow (K562) 108375288
chr19 5536480 5536946 SOX2 GTRD no Neural Stem Cells (H9) 108375289
chr19 5536491 5536875 SOX2 GTRD no Neural Stem Cells (H9) 108375290
chr19 5536513 5536897 TCF7L2 GTRD no Colon (HCT116) 108375291
chr19 5536657 5537013 ZNF143 GTRD no Epithelial (MCF-7) 108375293
chr19 5536752 5536767 TFAP2A JASPAR yes 70792555
chr19 5536752 5536767 TFAP2A JASPAR yes 112235602
chr19 5536754 5536769 TFAP2C JASPAR yes 70792556
chr19 5536754 5536769 TFAP2C JASPAR yes 112235603
chr19 5536755 5536767 TFAP2B JASPAR yes 70792557
chr19 5536755 5536767 TFAP2C JASPAR yes 70792558
chr19 5536755 5536767 TFAP2B JASPAR yes 112235604
chr19 5536755 5536767 TFAP2C JASPAR yes 112235605
chr19 5536756 5536765 TFAP2A JASPAR yes 70792559
chr19 5536756 5536765 TFAP2A JASPAR yes 112235606
chr19 5536760 5536765 SP1 TRANSFAC yes 70792560
chr19 5536760 5536765 SP1 TRANSFAC yes 112235607
Genes associated with rs766656[chr19:5536761], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. Start End Strand Gene name Ensembl ID TSS of gene Distance between TSS and SNP Tissue q Value id More