Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region



Chrom. Start End TF Name Source Predicted site? Tissue/Cell line id More
chr7 107950838 107950849 FOXB1 JASPAR yes 17127620
chr7 107950838 107950849 FOXB1 JASPAR yes 26114422
chr7 107950846 107950850 YY1 TRANSFAC yes 17127621
chr7 107950846 107950850 YY1 TRANSFAC yes 26114423
chr7 107950850 107950862 MYBL1 JASPAR yes 17127622
chr7 107950850 107950862 MYBL1 JASPAR yes 26114424
chr7 107950878 107950891 EOMES JASPAR yes 17127623
chr7 107950878 107950891 EOMES JASPAR yes 26114425
chr7 107950879 107950889 TBR1 JASPAR yes 17127624
chr7 107950879 107950889 TBR1 JASPAR yes 26114426
chr7 107950891 107950896 GATA2 JASPAR yes 17127625
chr7 107950891 107950896 GATA2 JASPAR yes 26114427
chr7 107950894 107950903 THAP1 JASPAR yes 17127626
chr7 107950894 107950903 THAP1 JASPAR yes 26114428
chr7 107950896 107950913 RARA JASPAR yes 17127627
chr7 107950896 107950913 RXRA JASPAR yes 17127628
chr7 107950896 107950913 RARA JASPAR yes 26114429
chr7 107950896 107950913 RXRA JASPAR yes 26114430
chr7 107950897 107950901 LFA1 TRANSFAC yes 17127629
chr7 107950897 107950901 LFA1 TRANSFAC yes 26114431
chr7 107950908 107950912 LFA1 TRANSFAC yes 17127630
chr7 107950908 107950912 LFA1 TRANSFAC yes 26114432
chr7 107950931 107950941 SP1 JASPAR yes 17127631
chr7 107950931 107950941 SP1 JASPAR yes 26114433
chr7 107950953 107950968 RUNX2 JASPAR yes 17127632
chr7 107950953 107950968 RUNX2 JASPAR yes 26114434
chr7 107950954 107950963 RUNX2 JASPAR yes 17127633
chr7 107950954 107950963 RUNX2 JASPAR yes 26114435
chr7 107950954 107950964 RUNX3 JASPAR yes 17127634
chr7 107950954 107950964 RUNX3 JASPAR yes 26114436
chr7 107950954 107950965 RUNX1 JASPAR yes 17127635
chr7 107950954 107950965 RUNX1 JASPAR yes 26114437
chr7 107950954 107950970 ZNF143 JASPAR yes 17127636
chr7 107950954 107950970 ZNF143 JASPAR yes 26114438
chr7 107950958 107950969 FOXH1 JASPAR yes 17127637
chr7 107950958 107950969 FOXH1 JASPAR yes 26114439
chr7 107950983 107950987 YY1 TRANSFAC yes 17127638
chr7 107950983 107950987 YY1 TRANSFAC yes 26114440
chr7 107950998 107951018 TP53 JASPAR yes 17127639
chr7 107950998 107951018 TP53 JASPAR yes 26114441
chr7 107951058 107951072 FOXF2 JASPAR yes 17127640
chr7 107951058 107951072 FOXF2 JASPAR yes 26114442
chr7 107951059 107951070 FOXC1 JASPAR yes 17127641
chr7 107951059 107951070 FOXC1 JASPAR yes 26114443
chr7 107951060 107951064 YY1 TRANSFAC yes 17127642
chr7 107951060 107951064 YY1 TRANSFAC yes 26114444
chr7 107951062 107951074 POU2F1 JASPAR yes 17127643
chr7 107951062 107951074 POU2F1 JASPAR yes 26114445
chr7 107951062 107951075 POU3F3 JASPAR yes 17127644
chr7 107951062 107951075 POU3F3 JASPAR yes 26114446
chr7 107951062 107951076 POU1F1 JASPAR yes 17127645
chr7 107951062 107951076 POU1F1 JASPAR yes 26114447
chr7 107951063 107951075 POU3F1 JASPAR yes 17127646
chr7 107951063 107951075 POU3F2 JASPAR yes 17127647
chr7 107951063 107951075 POU3F1 JASPAR yes 26114448
chr7 107951063 107951075 POU3F2 JASPAR yes 26114449
chr7 107951064 107951073 POU3F4 JASPAR yes 17127648
chr7 107951064 107951073 POU5F1B JASPAR yes 17127649
chr7 107951064 107951073 POU3F4 JASPAR yes 26114450
chr7 107951064 107951073 POU5F1B JASPAR yes 26114451
chr7 107951069 107951084 HNF4G JASPAR yes 17127650
chr7 107951069 107951084 NR2C2 JASPAR yes 17127651
chr7 107951069 107951084 HNF4G JASPAR yes 26114452
chr7 107951069 107951084 NR2C2 JASPAR yes 26114453
chr7 107951070 107951084 NR2F1 JASPAR yes 17127652
chr7 107951070 107951084 NR2F1 JASPAR yes 26114454
chr7 107951070 107951085 HNF4A JASPAR yes 17127653
chr7 107951070 107951085 HNF4A JASPAR yes 26114455
chr7 107951100 107951115 AR JASPAR yes 17127654
chr7 107951100 107951115 AR JASPAR yes 26114456
chr7 107951114 107951118 TEAD2 TRANSFAC yes 17127655
chr7 107951114 107951118 TEAD2 TRANSFAC yes 26114457
chr7 107951133 107951146 HSF1 JASPAR yes 17127656
chr7 107951133 107951146 HSF1 JASPAR yes 26114458
chr7 107951136 107951141 ETS2 TRANSFAC yes 17127657
chr7 107951136 107951141 ETS2 TRANSFAC yes 26114459

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr7 107950898 rs565164754 G C 10018397
chr7 107951006 rs145893037 T C
10018398
chr7 107951108 rs189815734 T A
10018399

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance between enhancer and TSS id More

No results

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand miRNA Name miRBase ID TSS Score TSI of Normal tissues TSI of Cancer tissues id More

No results