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 |
|---|---|---|---|---|---|---|---|
| chr1 | 918463 | rs72891194 | C | T | no | 1423 | |
| chr1 | 918464 | rs528144893 | G | A | no | 1424 | |
| chr1 | 918481 | rs143285747 | C | T |
|
1425 | |
| chr1 | 918532 | rs550919524 | G | A | no | 1426 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1 | 860260 | 879955 | + | SAMD11 | ENSG00000187634.6 | 860260 | 0.92 | 1.0 | 5 | 41811 | |
| chr1 | 861264 | 866445 | - | AL645608.1 | ENSG00000268179.1 | 866445 | 1.0 | 1.0 | 6 | 47996 | |
| chr1 | 879584 | 894689 | - | NOC2L | ENSG00000188976.6 | 894689 | 0.69 | 1.0 | 7 | 76240 | |
| chr1 | 895967 | 901095 | + | KLHL17 | ENSG00000187961.9 | 895967 | 0.67 | 1.0 | 8 | 77518 | |
| chr1 | 901877 | 911245 | + | PLEKHN1 | ENSG00000187583.6 | 901877 | 0.96 | 1.0 | 9 | 83428 | |
| chr1 | 910579 | 917497 | - | C1orf170 | ENSG00000187642.5 | 917497 | 0.99 | 1.0 | 10 | 99048 | |
| chr1 | 934342 | 935552 | - | HES4 | ENSG00000188290.6 | 935552 | 0.71 | 1.0 | 11 | 83003 | |
| chr1 | 948803 | 949920 | + | ISG15 | ENSG00000187608.5 | 948803 | 0.81 | 1.0 | 12 | 69752 | |
| chr1 | 955503 | 991496 | + | AGRN | ENSG00000188157.9 | 955503 | 0.91 | 1.0 | 13 | 63052 | |
| chr1 | 1006346 | 1009687 | - | RNF223 | ENSG00000237330.2 | 1009687 | 0.97 | 1.0 | 14 | 8868 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|