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
chr2 99723015 99723021 TBP TRANSFAC yes 22098668
chr2 99723016 99723031 STAT2 JASPAR yes 22098669
chr2 99723016 99723034 NR3C1 JASPAR yes 22098670
chr2 99723038 99723042 TEAD2 TRANSFAC yes 22098671
chr2 99723040 99723043 MYB TRANSFAC yes 22098672
chr2 99723047 99723053 NFIC JASPAR yes 22098673
chr2 99723049 99723053 H1TF2 TRANSFAC yes 22098674
chr2 99723049 99723053 NFE TRANSFAC yes 22098675
chr2 99723049 99723053 SRF TRANSFAC yes 22098676
chr2 99723056 99723061 ETS2 TRANSFAC yes 22098677
chr2 99723072 99723076 NFE TRANSFAC yes 22098678
chr2 99723074 99723084 SREBF1 JASPAR yes 22098679
chr2 99723074 99723084 SREBF2 JASPAR yes 22098680
chr2 99723090 99723103 SMAD2 JASPAR yes 22098681
chr2 99723092 99723113 ZNF263 JASPAR yes 22098682
chr2 99723098 99723113 NR2C2 JASPAR yes 22098683
chr2 99723100 99723111 E2F6 JASPAR yes 22098684
chr2 99723103 99723111 TBX15 JASPAR yes 22098685
chr2 99723114 99723124 TEAD4 JASPAR yes 22098686
chr2 99723135 99723138 MYB TRANSFAC yes 22098687
chr2 99723136 99723148 FOXI1 JASPAR yes 22098688
chr2 99723143 99723147 TEAD2 TRANSFAC yes 22098689
chr2 99723156 99723177 IRF1 JASPAR yes 22098690
chr2 99723158 99723173 STAT2 JASPAR yes 22098691
chr2 99723159 99723173 SPI1 JASPAR yes 22098692
chr2 99723178 99723182 YY1 TRANSFAC yes 22098693
chr2 99723223 99723228 ETS2 TRANSFAC yes 22098694
chr2 99723225 99723233 EHF JASPAR yes 22098695
chr2 99723231 99723245 TCF7L2 JASPAR yes 22098696
chr2 99723232 99723253 ZNF263 JASPAR yes 22098697
chr2 99723238 99723241 MYB TRANSFAC yes 22098698
chr2 99723257 99723261 NFE TRANSFAC yes 22098699
chr2 99723261 99723265 NFE TRANSFAC yes 22098700
chr2 99723268 99723274 SOX10 JASPAR yes 22098701
chr2 99723278 99723284 TCF1 TRANSFAC yes 22098702
chr2 99723308 99723312 TEAD2 TRANSFAC yes 22098703
chr2 99723310 99723313 MYB TRANSFAC yes 22098704
chr2 99723315 99723318 MYB TRANSFAC yes 22098705

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr2 99723016 rs34383742 TA T 5908021
chr2 99723016 rs796590535 TA T 5908022
chr2 99723040 rs375753340 A G
5908023
chr2 99723111 rs13008496 T C 5908024
chr2 99723210 rs60056452 C T no 5908025

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
chr2 99613724 99771427 - TSGA10 ENSG00000135951.10 99771427 0.8 1.0 2609 51921
chr2 99757948 99767950 + C2ORF15 ENSG00000273045.1 99757948 0.88 0.96 2611 65400
chr2 99757948 99939204 + C2orf15 ENSG00000241962.5 99757948 0.74 0.87 2610 65400
chr2 99771418 99779620 + LIPT1 ENSG00000144182.12 99771418 0.71 0.99 2612 51930
chr2 99771461 99811761 + MRPL30 ENSG00000273155.1 99771461 0.94 0.79 2613 51887
chr2 99777890 99797521 - MITD1 ENSG00000158411.6 99797521 0.73 0.98 2614 25827
chr2 99797542 99814089 + MRPL30 ENSG00000185414.15 99797542 0.84 0.75 2615 25806


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