EnhancerDB
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  3. rs12604076[chr17:76773638]
Enhancers that have rs12604076[chr17:76773638]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr17 76732944 76776375 enh17413
Liver Astrocyte Colon (HCT116) Pancreas Uterus Blood (T-cell) Stomach Skin (Keratinocyte) Brain (SK-N-SH) Blood (OCI-LY7) Peripheral Blood (MM.1S) Neural Stem Cells (H9) Thymus Prostate (PC-3) Esophagus Blood (GM12878) Placenta Lung (PC-9) Liver (HepG2) Prostate (RWPE1) Lung Muscle (A673) Heart
Transcript factors that have rs12604076[chr17:76773638]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr17 76772411 76773955 TCF7L2 GTRD no Colon (HCT116) 21795170
chr17 76772411 76773955 TCF7L2 GTRD no Colon (HCT116) 108304030
chr17 76772428 76774113 TCF7L2 GTRD no Colon (HCT116) 21795171
chr17 76772428 76774113 TCF7L2 GTRD no Colon (HCT116) 108304031
chr17 76772442 76773762 ZBTB33 GTRD no Brain (SK-N-SH) 21795172
chr17 76772442 76773762 ZBTB33 GTRD no Brain (SK-N-SH) 108304032
chr17 76772444 76773703 ZBTB33 GTRD no Brain (SK-N-SH) 21795173
chr17 76772444 76773703 ZBTB33 GTRD no Brain (SK-N-SH) 108304033
chr17 76773632 76773638 TCF4 TRANSFAC yes 56179291
chr17 76773633 76773645 FOXC2 JASPAR yes 56179292
Genes associated with rs12604076[chr17:76773638], 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