Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2 | 27530268 | 27531313 | - | UCN | ENSG00000163794.6 | 27531313 | 0.64 | 1.0 | 2216 | 1607 | |
| chr2 | 27532360 | 27548547 | - | MPV17 | ENSG00000115204.10 | 27548547 | 0.77 | 0.99 | 2217 | 18841 | |
| chr2 | 27548716 | 27579868 | - | GTF3C2 | ENSG00000115207.9 | 27579868 | 0.64 | 0.99 | 2218 | 50162 | |
| chr2 | 27587219 | 27593353 | - | EIF2B4 | ENSG00000115211.11 | 27593353 | 0.59 | 1.0 | 2219 | 63647 | |
| chr2 | 27593389 | 27599995 | + | SNX17 | ENSG00000115234.6 | 27593389 | 0.5 | 1.0 | 2220 | 63683 | |
| chr2 | 27600098 | 27603657 | - | ZNF513 | ENSG00000163795.9 | 27603657 | 0.65 | 1.0 | 2221 | 73951 | |
| chr2 | 27604061 | 27632554 | - | PPM1G | ENSG00000115241.9 | 27632554 | 0.56 | 0.99 | 2222 | 97216 | |
| chr2 | 27650657 | 27665126 | + | NRBP1 | ENSG00000115216.9 | 27650657 | 0.57 | 0.99 | 2223 | 79113 | |
| chr2 | 27665233 | 27669348 | + | KRTCAP3 | ENSG00000157992.8 | 27665233 | 0.82 | 1.0 | 2224 | 64537 | |
| chr2 | 27667238 | 27712656 | - | IFT172 | ENSG00000138002.10 | 27712656 | 0.76 | 1.0 | 2225 | 17114 | |
| chr2 | 27714750 | 27718112 | - | FNDC4 | ENSG00000115226.5 | 27718112 | 0.92 | 0.99 | 2226 | 11658 | |
| chr2 | 27719709 | 27746554 | + | GCKR | ENSG00000084734.4 | 27719709 | 0.99 | 0.97 | 2227 | 10061 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|