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 |
|---|---|---|---|---|---|---|---|
| chr17 | 27189743 | rs527711417 | A | G | no | 4813586 | |
| chr17 | 27189766 | rs552585884 | G | A,C | no | 4813587 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 27082996 | 27182250 | - | FAM222B | ENSG00000173065.9 | 27182250 | 0.67 | 1.0 | 15588 | 92548 | |
| chr17 | 27181956 | 27188085 | + | ERAL1 | ENSG00000132591.7 | 27181956 | 0.66 | 0.99 | 15589 | 92254 | |
| chr17 | 27206353 | 27224697 | - | FLOT2 | ENSG00000132589.11 | 27224697 | 0.7 | 1.0 | 15590 | 65072 | |
| chr17 | 27224799 | 27230089 | - | DHRS13 | ENSG00000167536.9 | 27230089 | 0.82 | 0.99 | 15591 | 59680 | |
| chr17 | 27232268 | 27278789 | - | PHF12 | ENSG00000109118.9 | 27278789 | 0.77 | 1.0 | 15592 | 10980 | |
| chr17 | 27277531 | 27384234 | + | PIPOX | ENSG00000179761.7 | 27277531 | 0.99 | 0.95 | 15593 | 12238 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17 | 27188566 | 27188585 | - | hsa-miR-144-3p | MIMAT0000436 | 27189006 | 0.15034965034965034 | 0.744907 | 0.0 | 681 | |
| chr17 | 27188686 | 27188706 | - | hsa-miR-4732-3p | MIMAT0019856 | 27189006 | 0.15034965034965034 | 0.0 | 0.0 | 683 |