Enhancers that have rs73449677[chr17:78500436]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 78498885 78507481 enh32372
chr17 78500391 78500494 vista26329

Transcript factors that have rs73449677[chr17:78500436]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 78499601 78501149 TCF7L2 GTRD no Colon (HCT116) 108307111
chr17 78499604 78500515 TCF7L2 GTRD no Colon (HCT116) 108307112
chr17 78499624 78500568 TCF7L2 GTRD no Colon (HCT116) 108307113
chr17 78499642 78500446 ZNF274 GTRD no Blood (GM12878) 108307114
chr17 78499660 78500444 TCF7L2 GTRD no Colon (HCT116) 108307115
chr17 78500383 78500599 ZNF143 ENCODE Uniform TFBS no Embryonic Stem Cell Line (H1-hESC) 108307116
chr17 78500421 78500436 TFAP2C JASPAR yes 21314766
chr17 78500421 78500436 TFAP2C JASPAR yes 56250296
chr17 78500434 78500439 SP1 TRANSFAC yes 21314768
chr17 78500434 78500439 SP1 TRANSFAC yes 56250298

Genes associated with rs73449677[chr17:78500436], 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