Enhancers that have rs117200430[chr12:66169894]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr12 66168947 66177881 enh58441

Transcript factors that have rs117200430[chr12:66169894]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr12 66168932 66170345 TCF7L2 GTRD no Colon (HCT116) 21553364
chr12 66169051 66170334 TCF7L2 GTRD no Colon (HCT116) 21553365
chr12 66169090 66170195 TCF7L2 GTRD no Colon (HCT116) 21553366
chr12 66169096 66170156 ERG GTRD no Prostate (RWPE1) 21553367
chr12 66169211 66170381 TCF7L2 GTRD no Colon (HCT116) 21553368
chr12 66169225 66170576 TCF7L2 GTRD no Colon (HCT116) 21553369
chr12 66169250 66170408 TCF7L2 GTRD no Colon (HCT116) 21553370
chr12 66169253 66170147 TCF7L2 GTRD no Colon (HCT116) 21553371
chr12 66169268 66170625 TCF7L2 GTRD no Colon (HCT116) 21553372
chr12 66169307 66170325 TCF7L2 GTRD no Colon (HCT116) 21553373
chr12 66169328 66170556 TCF7L2 GTRD no Colon (HCT116) 21553374
chr12 66169341 66170571 TCF7L2 GTRD no Colon (HCT116) 21553375
chr12 66169377 66170381 TCF7L2 GTRD no Colon (HCT116) 21553376
chr12 66169437 66170210 TCF7L2 GTRD no Colon (HCT116) 21553377
chr12 66169481 66170577 TCF7L2 GTRD no Colon (HCT116) 21553378
chr12 66169800 66170377 P63 GTRD no Skin (Keratinocyte) 21553379

Genes associated with rs117200430[chr12:66169894], 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