EnhancerDB
  1. Home
  2. SNP
  3. rs35727368[chr16:89050706]
Enhancers that have rs35727368[chr16:89050706]
Back to top
Chrom. Start End Enhancer ID Tissues that enhancer appears More
chr16 89046288 89055611 enh47987
Thymus Blood (OCI-LY7)
chr16 89050571 89050973 vista23541
VISTA
Transcript factors that have rs35727368[chr16:89050706]
Back to top
Chrom. Start End TF name Source Predicted site? Tissue id More
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224658
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224659
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224660
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224661
chr16 89047034 89056300 TCF7L2 GTRD no Colon (HCT116) 108224662
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224663
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224664
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224665
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224666
chr16 89047135 89056347 TCF7L2 GTRD no Colon (HCT116) 108224667
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224670
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224671
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224672
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224673
chr16 89047179 89056338 TCF7L2 GTRD no Colon (HCT116) 108224674
chr16 89049905 89055158 TCF7L2 GTRD no Colon (HCT116) 108224741
chr16 89049905 89055158 TCF7L2 GTRD no Colon (HCT116) 108224742
chr16 89049905 89055158 TCF7L2 GTRD no Colon (HCT116) 108224743
chr16 89050476 89050731 ZNF274 GTRD no Blood (GM12878) 108224756
chr16 89050574 89052014 TCF7L2 GTRD no Colon (HCT116) 108224757
chr16 89050596 89051452 TCF7L2 GTRD no Colon (HCT116) 108224758
chr16 89050695 89050710 HSF1 JASPAR yes 12313117
chr16 89050695 89050710 HSF1 JASPAR yes 49419934
chr16 89050696 89050709 HSF1 JASPAR yes 12313118
chr16 89050696 89050709 HSF2 JASPAR yes 12313119
chr16 89050696 89050709 HSF4 JASPAR yes 12313120
chr16 89050696 89050709 HSF1 JASPAR yes 49419935
chr16 89050696 89050709 HSF2 JASPAR yes 49419936
chr16 89050696 89050709 HSF4 JASPAR yes 49419937
chr16 89050700 89050715 HSF1 JASPAR yes 12313121
chr16 89050700 89050715 HSF1 JASPAR yes 49419938
chr16 89050701 89050714 HSF1 JASPAR yes 12313122
chr16 89050701 89050714 HSF2 JASPAR yes 12313123
chr16 89050701 89050714 HSF4 JASPAR yes 12313124
chr16 89050701 89050714 HSF1 JASPAR yes 49419939
chr16 89050701 89050714 HSF2 JASPAR yes 49419940
chr16 89050701 89050714 HSF4 JASPAR yes 49419941
chr16 89050705 89050720 HSF1 JASPAR yes 12313125
chr16 89050705 89050720 HSF1 JASPAR yes 49419942
chr16 89050706 89050719 HSF1 JASPAR yes 12313126
chr16 89050706 89050719 HSF2 JASPAR yes 12313127
chr16 89050706 89050719 HSF4 JASPAR yes 12313128
chr16 89050706 89050719 HSF1 JASPAR yes 49419943
chr16 89050706 89050719 HSF2 JASPAR yes 49419944
chr16 89050706 89050719 HSF4 JASPAR yes 49419945
Genes associated with rs35727368[chr16:89050706], comfirmed by eQTL
Back to top
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