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
chr13 113946410 113946668 EGR1 UCSC Txn Factor no Conserved 108091105
chr13 113946286 113946298 GRHL1 JASPAR yes 19347669
chr13 113946287 113946297 TFCP2 JASPAR yes 19347670
chr13 113946291 113946296 MYC TRANSFAC yes 19347671
chr13 113946293 113946308 MEF2C JASPAR yes 19347672
chr13 113946294 113946309 MEF2A JASPAR yes 19347673
chr13 113946318 113946324 TCF4 TRANSFAC yes 19347674
chr13 113946333 113946347 RORA JASPAR yes 19347675
chr13 113946336 113946351 JUND JASPAR yes 19347676
chr13 113946339 113946345 ESR1 TRANSFAC yes 19347677
chr13 113946341 113946345 ESR1 TRANSFAC yes 19347678
chr13 113946354 113946374 RREB1 JASPAR yes 19347679
chr13 113946381 113946386 TFAP2A TRANSFAC yes 19347680
chr13 113946381 113946387 MZF1 JASPAR yes 19347681
chr13 113946460 113946463 MYB TRANSFAC yes 19347682
chr13 113946467 113946477 TFCP2 JASPAR yes 19347683
chr13 113946495 113946509 PLAG1 JASPAR yes 19347684
chr13 113946519 113946530 E2F4 JASPAR yes 19347685
chr13 113946521 113946531 SP1 JASPAR yes 19347686
chr13 113946522 113946528 SP1 TRANSFAC yes 19347687
chr13 113946522 113946532 SP1 JASPAR yes 19347688
chr13 113946523 113946530 SP1 TRANSFAC yes 19347689
chr13 113946524 113946529 SP1 TRANSFAC yes 19347690
chr13 113946524 113946530 SP1 TRANSFAC yes 19347691
chr13 113946524 113946531 SP1 TRANSFAC yes 19347692
chr13 113946525 113946533 WT1 TRANSFAC yes 19347693
chr13 113946532 113946543 E2F1 JASPAR yes 19347694
chr13 113946536 113946541 SP1 TRANSFAC yes 19347695
chr13 113946542 113946547 SP1 TRANSFAC yes 19347696
chr13 113946546 113946558 HINFP JASPAR yes 19347697
chr13 113946598 113946619 ZNF263 JASPAR yes 19347698
chr13 113946606 113946620 SPI1 JASPAR yes 19347699
chr13 113946606 113946620 SPIC JASPAR yes 19347700
chr13 113946607 113946615 EHF JASPAR yes 19347701
chr13 113946640 113946646 LEF1 TRANSFAC yes 19347702
chr13 113946640 113946646 SOX10 JASPAR yes 19347703

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr13 113946352 rs566660191 G A,T no 3409414
chr13 113946374 rs558418976 A G
3409415
chr13 113946412 rs556970636 T G
3409416
chr13 113946466 rs368797532 T C
3409417
chr13 113946483 rs1078712 A C,G
3409418
chr13 113946499 rs115350215 C T
3409419
chr13 113946527 rs1078711 G A 3409420
chr13 113946532 rs565554354 C T 3409421
chr13 113946535 rs532888920 T C
3409422
chr13 113946563 rs1078710 A C
3409423
chr13 113946631 rs185458190 C G,T
3409424

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
chr13 113831891 113863029 - PCID2 ENSG00000126226.17 113863029 0.57 1.0 13040 16753
chr13 113862552 113919399 + CUL4A ENSG00000139842.10 113862552 0.57 0.99 13041 16276
chr13 113951556 113977987 + LAMP1 ENSG00000185896.9 113951556 0.63 1.0 13042 95092
chr13 113978505 114018446 - GRTP1 ENSG00000139835.9 114018446 0.89 1.0 13043 28202


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