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
chr9 34193362 34193369 SPIB JASPAR yes 83831807
chr9 34193362 34193369 SPIB JASPAR yes 95346950
chr9 34193372 34193382 SREBF1 JASPAR yes 83831808
chr9 34193372 34193382 SREBF1 JASPAR yes 95346951
chr9 34193373 34193381 MGA JASPAR yes 83831809
chr9 34193373 34193381 MGA JASPAR yes 95346952
chr9 34193376 34193396 RREB1 JASPAR yes 83831810
chr9 34193376 34193396 RREB1 JASPAR yes 95346953
chr9 34193377 34193392 RUNX2 JASPAR yes 83831811
chr9 34193377 34193392 RUNX2 JASPAR yes 95346954
chr9 34193383 34193395 PBX1 JASPAR yes 83831812
chr9 34193383 34193395 PBX1 JASPAR yes 95346955
chr9 34193403 34193416 ZBTB18 JASPAR yes 83831813
chr9 34193403 34193416 ZBTB18 JASPAR yes 95346956
chr9 34193421 34193431 ZNF740 JASPAR yes 83831814
chr9 34193421 34193431 ZNF740 JASPAR yes 95346957
chr9 34193426 34193436 REL JASPAR yes 83831815
chr9 34193426 34193436 REL JASPAR yes 95346958
chr9 34193426 34193437 NFKB1 JASPAR yes 83831816
chr9 34193426 34193437 NFKB1 JASPAR yes 95346959
chr9 34193434 34193448 RXRG JASPAR yes 83831817
chr9 34193434 34193448 RXRG JASPAR yes 95346960
chr9 34193434 34193449 NR2C2 JASPAR yes 83831818
chr9 34193434 34193449 NR2C2 JASPAR yes 95346961
chr9 34193474 34193478 H1TF2 TRANSFAC yes 83831819
chr9 34193474 34193478 NFE TRANSFAC yes 83831820
chr9 34193474 34193478 SRF TRANSFAC yes 83831821
chr9 34193474 34193478 H1TF2 TRANSFAC yes 95346962
chr9 34193474 34193478 NFE TRANSFAC yes 95346963
chr9 34193474 34193478 SRF TRANSFAC yes 95346964
chr9 34193527 34193532 MYC TRANSFAC yes 83831822
chr9 34193527 34193532 MYC TRANSFAC yes 95346965
chr9 34193540 34193545 SP1 TRANSFAC yes 83831823
chr9 34193540 34193545 SP1 TRANSFAC yes 95346966
chr9 34193555 34193569 RORA JASPAR yes 83831824
chr9 34193555 34193569 RORA JASPAR yes 95346967
chr9 34193563 34193567 NFE TRANSFAC yes 83831825
chr9 34193563 34193567 NFE TRANSFAC yes 95346968

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr9 34193468 rs141832385 G T no 10999503
chr9 34193478 rs187327033 A G
10999504
chr9 34193535 rs74716638 A G no 10999505

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
chr9 34086385 34127397 - DCAF12 ENSG00000198876.8 34127397 0.65 0.99 8893 34048
chr9 34179003 34252521 + UBAP1 ENSG00000165006.9 34179003 0.6 1.0 8894 85654


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