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
chr14 71022244 71022258 PAX6 JASPAR yes 107576651
chr14 71022252 71022256 YY1 TRANSFAC yes 107576652
chr14 71022258 71022276 SRF JASPAR yes 107576653
chr14 71022281 71022293 MEF2A JASPAR yes 107576654
chr14 71022281 71022293 MEF2D JASPAR yes 107576655
chr14 71022313 71022321 FOXO3 JASPAR yes 107576656
chr14 71022325 71022330 MYB TRANSFAC yes 107576657
chr14 71022332 71022353 IRF1 JASPAR yes 107576658
chr14 71022334 71022349 STAT2 JASPAR yes 107576659
chr14 71022341 71022355 SPIC JASPAR yes 107576660
chr14 71022364 71022368 YY1 TRANSFAC yes 107576661
chr14 71022364 71022378 PAX6 JASPAR yes 107576662
chr14 71022368 71022378 TBX21 JASPAR yes 107576663
chr14 71022368 71022379 TBX2 JASPAR yes 107576664
chr14 71022368 71022381 EOMES JASPAR yes 107576665
chr14 71022369 71022379 TBR1 JASPAR yes 107576666
chr14 71022386 71022393 GATA1 TRANSFAC yes 107576667
chr14 71022389 71022393 TEAD2 TRANSFAC yes 107576668
chr14 71022393 71022403 NFATC3 JASPAR yes 107576669
chr14 71022394 71022401 NFATC2 JASPAR yes 107576670
chr14 71022455 71022469 POU1F1 JASPAR yes 107576671
chr14 71022456 71022468 POU3F1 JASPAR yes 107576672
chr14 71022456 71022468 POU3F2 JASPAR yes 107576673
chr14 71022456 71022469 POU3F3 JASPAR yes 107576674
chr14 71022457 71022467 NFATC3 JASPAR yes 107576675
chr14 71022464 71022474 SREBF1 JASPAR yes 107576676
chr14 71022464 71022474 SREBF2 JASPAR yes 107576677
chr14 71022488 71022492 NFE TRANSFAC yes 107576678
chr14 71022492 71022513 ZNF263 JASPAR yes 107576679
chr14 71022508 71022529 ZNF263 JASPAR yes 107576680
chr14 71022517 71022531 SPI1 JASPAR yes 107576681
chr14 71022533 71022542 NKX3-2 JASPAR yes 107576682
chr14 71022538 71022553 STAT2 JASPAR yes 107576683
chr14 71022540 71022555 IRF9 JASPAR yes 107576684
chr14 71022562 71022570 FOXO3 JASPAR yes 107576685

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr14 71022298 rs76908228 C A no 3640657
chr14 71022311 rs145489091 C G no 3640658
chr14 71022327 rs8018765 T C
3640659
chr14 71022329 rs140703650 G GA
3640660
chr14 71022411 rs148850266 A T no 3640661
chr14 71022429 rs187614426 C T no 3640662
chr14 71022435 rs72719745 T C no 3640663
chr14 71022436 rs567504940 TTC T no 3640664

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
chr14 70989075 71001732 - ADAM20 ENSG00000134007.3 71001732 0.88 0.95 13441 79514
chr14 71047974 71067384 - MED6 ENSG00000133997.7 71067384 0.64 0.98 13442 55186
chr14 71108504 71142077 + TTC9 ENSG00000133985.2 71108504 0.89 1.0 13443 14066


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