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
chr17 27359789 27359810 IRF1 JASPAR yes 21214403
chr17 27359789 27359810 IRF1 JASPAR yes 53709588
chr17 27359793 27359808 PRDM1 JASPAR yes 21214404
chr17 27359793 27359808 STAT2 JASPAR yes 21214405
chr17 27359793 27359808 PRDM1 JASPAR yes 53709589
chr17 27359793 27359808 STAT2 JASPAR yes 53709590
chr17 27359795 27359816 IRF1 JASPAR yes 21214406
chr17 27359795 27359816 IRF1 JASPAR yes 53709591
chr17 27359799 27359814 PRDM1 JASPAR yes 21214407
chr17 27359799 27359814 PRDM1 JASPAR yes 53709592
chr17 27359835 27359842 NFATC2 JASPAR yes 21214408
chr17 27359835 27359842 NFATC2 JASPAR yes 53709593
chr17 27359848 27359854 NFIC JASPAR yes 21214409
chr17 27359848 27359854 NFIC JASPAR yes 53709594
chr17 27359858 27359869 TBX20 JASPAR yes 21214410
chr17 27359858 27359869 TBX20 JASPAR yes 53709595
chr17 27359859 27359867 TBX15 JASPAR yes 21214411
chr17 27359859 27359867 TBX15 JASPAR yes 53709596
chr17 27359860 27359865 SP1 TRANSFAC yes 21214412
chr17 27359860 27359865 SP1 TRANSFAC yes 53709597
chr17 27359863 27359868 ETS2 TRANSFAC yes 21214413
chr17 27359863 27359868 ETS2 TRANSFAC yes 53709598
chr17 27359876 27359881 MYC TRANSFAC yes 21214414
chr17 27359876 27359881 MYC TRANSFAC yes 53709599
chr17 27359887 27359891 TEAD2 TRANSFAC yes 21214415
chr17 27359887 27359891 TEAD2 TRANSFAC yes 53709600
chr17 27359896 27359908 NHLH1 JASPAR yes 21214416
chr17 27359896 27359908 NHLH1 JASPAR yes 53709601
chr17 27359908 27359923 ZIC3 JASPAR yes 21214417
chr17 27359908 27359923 ZIC4 JASPAR yes 21214418
chr17 27359908 27359923 ZIC3 JASPAR yes 53709602
chr17 27359908 27359923 ZIC4 JASPAR yes 53709603
chr17 27359909 27359923 ZIC1 JASPAR yes 21214419
chr17 27359909 27359923 ZIC1 JASPAR yes 53709604
chr17 27359918 27359922 H4TF2 TRANSFAC yes 21214420
chr17 27359918 27359922 H4TF2 TRANSFAC yes 53709605
chr17 27359984 27360005 ZNF263 JASPAR yes 21214421
chr17 27359984 27360005 ZNF263 JASPAR yes 53709606
chr17 27359985 27359996 FLI1 JASPAR yes 21214422
chr17 27359985 27359996 FLI1 JASPAR yes 53709607
chr17 27359986 27359996 GABPA JASPAR yes 21214423
chr17 27359986 27359996 GABPA JASPAR yes 53709608
chr17 27359986 27359999 ELF1 JASPAR yes 21214424
chr17 27359986 27359999 ELF1 JASPAR yes 53709609
chr17 27359987 27359994 SPI1 JASPAR yes 21214425
chr17 27359987 27359994 SPI1 JASPAR yes 53709610
chr17 27359987 27359995 FEV JASPAR yes 21214426
chr17 27359987 27359995 FEV JASPAR yes 53709611
chr17 27359989 27359994 ETS2 TRANSFAC yes 21214427
chr17 27359989 27359994 ETS2 TRANSFAC yes 53709612
chr17 27360005 27360018 HSF2 JASPAR yes 21214428
chr17 27360005 27360018 HSF2 JASPAR yes 53709613
chr17 27360007 27360017 NFATC3 JASPAR yes 21214429
chr17 27360007 27360017 NFATC3 JASPAR yes 53709614
chr17 27360008 27360015 NFATC2 JASPAR yes 21214430
chr17 27360008 27360015 NFATC2 JASPAR yes 53709615
chr17 27360009 27360022 ZBTB18 JASPAR yes 21214431
chr17 27360009 27360022 ZBTB18 JASPAR yes 53709616
chr17 27360018 27360032 MTF1 JASPAR yes 21214432
chr17 27360018 27360032 MTF1 JASPAR yes 53709617
chr17 27360026 27360040 RXRB JASPAR yes 21214433
chr17 27360026 27360040 RXRG JASPAR yes 21214434
chr17 27360026 27360040 RXRB JASPAR yes 53709618
chr17 27360026 27360040 RXRG JASPAR yes 53709619
chr17 27360026 27360041 NR2C2 JASPAR yes 21214435
chr17 27360026 27360041 NR2C2 JASPAR yes 53709620
chr17 27360027 27360043 SOX4 JASPAR yes 21214436
chr17 27360027 27360043 SOX4 JASPAR yes 53709621
chr17 27360031 27360040 ZEB1 JASPAR yes 21214437
chr17 27360031 27360040 ZEB1 JASPAR yes 53709622
chr17 27360034 27360039 USF2 TRANSFAC yes 21214438
chr17 27360034 27360039 USF2 TRANSFAC yes 53709623
chr17 27360054 27360065 FOXH1 JASPAR yes 21214439
chr17 27360054 27360065 FOXH1 JASPAR yes 53709624
chr17 27360055 27360061 ZNF354C JASPAR yes 21214440
chr17 27360055 27360061 ZNF354C JASPAR yes 53709625
chr17 27360058 27360063 H4TF1 TRANSFAC yes 21214441
chr17 27360058 27360063 H4TF1 TRANSFAC yes 53709626

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr17 27359832 rs78591747 C G no 4814449
chr17 27359903 rs115451385 C T
4814450

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
chr17 27232268 27278789 - PHF12 ENSG00000109118.9 27278789 0.77 1.0 15592 18981
chr17 27277531 27384234 + PIPOX ENSG00000179761.7 27277531 0.99 0.95 15593 17723
chr17 27281919 27333458 - SEZ6 ENSG00000063015.15 27333458 0.83 1.0 15594 73650
chr17 27400537 27418537 - TIAF1 ENSG00000221995.4 27418537 0.68 0.99 15596 41528


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