Enhancers that have rs4906030[chr14:101458641]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr14 101443405 101463335 enh58625

Transcript factors that have rs4906030[chr14:101458641]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr14 101457131 101459690 TCF7L2 GTRD no Colon (HCT116) 21640439
chr14 101457285 101458720 TCF7L2 GTRD no Colon (HCT116) 21640444
chr14 101457806 101458705 TCF7L2 GTRD no Colon (HCT116) 21640449
chr14 101458173 101458739 TCF7L2 GTRD no Colon (HCT116) 21640450
chr14 101458208 101459050 TCF7L2 GTRD no Colon (HCT116) 21640451
chr14 101458257 101459217 TCF7L2 GTRD no Colon (HCT116) 21640452
chr14 101458448 101459315 TCF7L2 GTRD no Colon (HCT116) 21640453
chr14 101458590 101459700 TCF7L2 GTRD no Colon (HCT116) 21640454
chr14 101458610 101458996 TCF7L2 GTRD no Colon (HCT116) 21640455

Genes associated with rs4906030[chr14:101458641], 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