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 |
|---|---|---|---|---|---|---|---|---|
| chr19 | 49486710 | 49487073 | SIX5 | UCSC Txn Factor | no | Conserved | 108422500 | |
| chr19 | 49486759 | 49487035 | ZNF143 | UCSC Txn Factor | no | Conserved | 108422507 | |
| chr19 | 49486900 | 49486918 | NFYA | JASPAR | yes | 70866169 | ||
| chr19 | 49486901 | 49486904 | MYB | TRANSFAC | yes | 70866170 | ||
| chr19 | 49486910 | 49486926 | ZNF143 | JASPAR | yes | 70866171 | ||
| chr19 | 49486929 | 49486942 | EOMES | JASPAR | yes | 70866172 | ||
| chr19 | 49486931 | 49486941 | TBR1 | JASPAR | yes | 70866173 | ||
| chr19 | 49486931 | 49486942 | TBX2 | JASPAR | yes | 70866174 | ||
| chr19 | 49486932 | 49486942 | TBX21 | JASPAR | yes | 70866175 | ||
| chr19 | 49486951 | 49486966 | STAT2 | JASPAR | yes | 70866176 | ||
| chr19 | 49486957 | 49486962 | GATA2 | JASPAR | yes | 70866177 | ||
| chr19 | 49486957 | 49486974 | ZNF410 | JASPAR | yes | 70866178 | ||
| chr19 | 49486971 | 49486976 | ETS2 | TRANSFAC | yes | 70866179 | ||
| chr19 | 49486971 | 49486983 | TEAD1 | JASPAR | yes | 70866180 | ||
| chr19 | 49486978 | 49486987 | HIC2 | JASPAR | yes | 70866181 | ||
| chr19 | 49486994 | 49486997 | MYB | TRANSFAC | yes | 70866182 | ||
| chr19 | 49487004 | 49487019 | HNF4G | JASPAR | yes | 70866183 | ||
| chr19 | 49487005 | 49487019 | NR2F1 | JASPAR | yes | 70866184 | ||
| chr19 | 49487005 | 49487020 | HNF4A | JASPAR | yes | 70866185 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19 | 49384222 | 49401990 | - | TULP2 | ENSG00000104804.3 | 49401990 | 0.8 | 0.99 | 17807 | 15100 | |
| chr19 | 49403307 | 49426629 | + | NUCB1 | ENSG00000104805.11 | 49403307 | 0.69 | 1.0 | 17808 | 16417 | |
| chr19 | 49436939 | 49448226 | + | DHDH | ENSG00000104808.3 | 49436939 | 0.96 | 1.0 | 17809 | 50049 | |
| chr19 | 49458072 | 49465055 | + | BAX | ENSG00000087088.15 | 49458072 | 0.66 | 0.99 | 17810 | 71182 | |
| chr19 | 49468558 | 49470135 | + | FTL | ENSG00000087086.9 | 49468558 | 0.88 | 0.99 | 17811 | 81668 | |
| chr19 | 49471382 | 49496567 | - | GYS1 | ENSG00000104812.10 | 49496567 | 0.66 | 1.0 | 17812 | 90461 | |
| chr19 | 49496705 | 49519252 | + | RUVBL2 | ENSG00000183207.8 | 49496705 | 0.79 | 1.0 | 17813 | 90323 | |
| chr19 | 49519237 | 49520338 | - | LHB | ENSG00000104826.7 | 49520338 | 0.96 | 1.0 | 17814 | 66690 | |
| chr19 | 49526126 | 49527590 | - | CGB | ENSG00000104827.12 | 49527590 | 1.0 | 1.0 | 17815 | 59438 | |
| chr19 | 49526210 | 49540152 | - | CTB-60B18.6 | ENSG00000267335.2 | 49540152 | 0.98 | 0.87 | 17816 | 46876 | |
| chr19 | 49535169 | 49536495 | + | CGB2 | ENSG00000104818.14 | 49535169 | 0.99 | 1.0 | 17817 | 51859 | |
| chr19 | 49538831 | 49552006 | - | CGB1 | ENSG00000267631.3 | 49552006 | 0.98 | 0.93 | 17818 | 35022 | |
| chr19 | 49547141 | 49548568 | + | CGB5 | ENSG00000189052.6 | 49547141 | 1.0 | 1.0 | 17819 | 39887 | |
| chr19 | 49550895 | 49552400 | - | CGB8 | ENSG00000213030.4 | 49552400 | 1.0 | 0.99 | 17820 | 34628 | |
| chr19 | 49557531 | 49562117 | - | CGB7 | ENSG00000196337.6 | 49562117 | 0.91 | 1.0 | 17821 | 24911 | |
| chr19 | 49559050 | 49568333 | - | NTF4 | ENSG00000225950.3 | 49568333 | 0.87 | 1.0 | 17822 | 18695 | |
| chr19 | 49570675 | 49576198 | - | KCNA7 | ENSG00000104848.1 | 49576198 | 0.96 | 1.0 | 17823 | 10830 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|