EnhancerDB
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  3. rs568900553[chr16:89381259]
Enhancers that have rs568900553[chr16:89381259]
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Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 89371847 89409975 enh16905
Bone Marrow (K562) Liver Colon (HCT116) Adrenal Embryonic Stem Cell Line (H1-hESC) Pancreas Uterus Blood (T-cell) Epithelial (MCF-7) Stomach Brain (SK-N-SH) Ovary Bone (Osteoblast) Blood (OCI-LY7) Lung (A549) Thyroid Peripheral Blood (MM.1S) Pancreas (Panc1) Neural Stem Cells (H9) Thymus Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Esophagus Blood (GM12878) Placenta Lung (PC-9) Muscle (Myoblast) Spleen Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Lung Muscle (A673) Heart
Transcript factors that have rs568900553[chr16:89381259]
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Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 89380522 89381458 TCF7L2 GTRD no Colon (HCT116) 21738057
chr16 89380522 89381458 TCF7L2 GTRD no Colon (HCT116) 108225500
chr16 89380660 89381327 TCF7L2 GTRD no Colon (HCT116) 21738060
chr16 89380660 89381327 TCF7L2 GTRD no Colon (HCT116) 108225503
chr16 89381253 89381264 GCM1 JASPAR yes 12330044
chr16 89381255 89381264 THAP1 JASPAR yes 12330045
chr16 89381258 89381262 LFA1 TRANSFAC yes 12330046
chr16 89381259 89382306 ZNF274 GTRD no Blood (GM12878) 21738063
chr16 89381259 89382306 ZNF274 GTRD no Blood (GM12878) 108225506
Genes associated with rs568900553[chr16:89381259], 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