Enhancers that have rs534208002[chr16:1210538]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 1204345 1228235 enh31663
chr16 1210403 1210717 vista21539

Transcript factors that have rs534208002[chr16:1210538]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 1209544 1210678 TCF7L2 GTRD no Colon (HCT116) 21684323
chr16 1209544 1210678 TCF7L2 GTRD no Colon (HCT116) 108171264
chr16 1209544 1210678 TCF7L2 GTRD no Colon (HCT116) 108171265
chr16 1209793 1210688 TCF7L2 GTRD no Colon (HCT116) 21684324
chr16 1209793 1210688 TCF7L2 GTRD no Colon (HCT116) 108171266
chr16 1209822 1210636 TCF7L2 GTRD no Colon (HCT116) 21684325
chr16 1209822 1210636 TCF7L2 GTRD no Colon (HCT116) 108171267
chr16 1210039 1211346 TCF7L2 GTRD no Colon (HCT116) 21684326
chr16 1210039 1211346 TCF7L2 GTRD no Colon (HCT116) 108171268
chr16 1210171 1210642 ZNF274 GTRD no Bone Marrow (K562) 108171270
chr16 1210188 1210634 ZNF274 GTRD no Bone Marrow (K562) 108171271
chr16 1210330 1210666 ZNF274 GTRD no Bone Marrow (K562) 108171272
chr16 1210377 1210615 ZBTB33 GTRD no Brain (SK-N-SH) 108171273
chr16 1210531 1210540 HIC2 JASPAR yes 9139800
chr16 1210531 1210540 HIC2 JASPAR yes 49326136

Genes associated with rs534208002[chr16:1210538], 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