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 69377332 69377351 REST JASPAR yes 107573485
chr14 69377359 69377374 RUNX2 JASPAR yes 107573486
chr14 69377360 69377369 RUNX2 JASPAR yes 107573487
chr14 69377360 69377370 RUNX3 JASPAR yes 107573488
chr14 69377360 69377371 RUNX1 JASPAR yes 107573489
chr14 69377360 69377380 RREB1 JASPAR yes 107573490
chr14 69377369 69377383 GLIS3 JASPAR yes 107573491
chr14 69377393 69377407 E2F7 JASPAR yes 107573492
chr14 69377395 69377405 SP1 JASPAR yes 107573493
chr14 69377396 69377402 SP1 TRANSFAC yes 107573494
chr14 69377396 69377406 SP1 JASPAR yes 107573495
chr14 69377398 69377403 SP1 TRANSFAC yes 107573496
chr14 69377404 69377415 DUX4 JASPAR yes 107573497
chr14 69377425 69377441 ZNF143 JASPAR yes 107573498
chr14 69377436 69377446 CLOCK JASPAR yes 107573499
chr14 69377436 69377446 MAX JASPAR yes 107573500
chr14 69377437 69377444 USF1 JASPAR yes 107573501
chr14 69377437 69377447 MAX JASPAR yes 107573502
chr14 69377438 69377443 MYC TRANSFAC yes 107573503
chr14 69377438 69377443 USF1 TRANSFAC yes 107573504
chr14 69377438 69377443 USF2 TRANSFAC yes 107573505
chr14 69377448 69377461 SMAD2 JASPAR yes 107573506
chr14 69377459 69377464 SP1 TRANSFAC yes 107573507
chr14 69377467 69377480 DUXA JASPAR yes 107573508
chr14 69377479 69377489 SP1 JASPAR yes 107573509
chr14 69377489 69377501 INSM1 JASPAR yes 107573510
chr14 69377490 69377500 MZF1 JASPAR yes 107573511
chr14 69377518 69377533 ZBTB33 JASPAR yes 107573512
chr14 69377521 69377536 ZBTB33 JASPAR yes 107573513
chr14 69377547 69377560 NFKB1 JASPAR yes 107573514
chr14 69377547 69377560 NFKB2 JASPAR yes 107573515
chr14 69377548 69377559 NFKB1 JASPAR yes 107573516
chr14 69377549 69377559 NFKB1 JASPAR yes 107573517
chr14 69377549 69377559 RELA JASPAR yes 107573518
chr14 69377549 69377560 NFKB1 JASPAR yes 107573519
chr14 69377555 69377570 PRDM1 JASPAR yes 107573520
chr14 69377599 69377603 H4TF2 TRANSFAC yes 107573521

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr14 69377376 rs144970331 CCT C
3630338
chr14 69377377 rs559659271 C G
3630339
chr14 69377380 rs60268202 C T
3630340
chr14 69377385 rs7157253 T C no 3630341
chr14 69377412 rs549612289 A G
3630342
chr14 69377431 rs145864062 A G
3630343
chr14 69377455 rs182493104 G A
3630344
chr14 69377458 rs7155870 A C
3630345
chr14 69377528 rs113516265 C T
3630346
chr14 69377534 rs146986774 C T
3630347

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 69340860 69446157 - ACTN1 ENSG00000072110.9 69446157 0.88 1.0 13424 31453


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