EnhancerDB
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  3. rs376938738[chr16:87897592]
Enhancers that have rs376938738[chr16:87897592]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 87873744 87902035 enh4182
Bone Marrow (K562) Astrocyte Colon (HCT116) Blood (Karpas-422) Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Blood (T-cell) Stomach Brain (SK-N-SH) Bone (Osteoblast) Blood (OCI-LY7) Pancreas (Panc1) Neural Stem Cells (H9) Prostate (PC-3) Cervix (HeLa-S3) Esophagus Blood (GM12878) Placenta Lung (PC-9) Muscle (Myoblast) Liver (HepG2) Muscle (A673) Heart
Transcript factors that have rs376938738[chr16:87897592]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 87895470 87898057 ZNF274 GTRD no Liver (HepG2) 21735346
chr16 87896749 87898184 TCF7L2 GTRD no Colon (HCT116) 21735347
chr16 87896805 87898330 ZNF274 GTRD no Blood (GM12878) 21735348
chr16 87896950 87898450 TCF7L2 GTRD no Colon (HCT116) 21735349
chr16 87897521 87898195 ZNF274 GTRD no Liver (HepG2) 21735350
chr16 87897583 87897598 MEF2C JASPAR yes 12249037
chr16 87897584 87897599 MEF2A JASPAR yes 12249038
chr16 87897585 87897597 MEF2A JASPAR yes 12249039
chr16 87897586 87897596 MEF2A JASPAR yes 12249040
chr16 87897592 87897603 FOXB1 JASPAR yes 12249041
Genes associated with rs376938738[chr16:87897592], 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