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 |
|---|---|---|---|---|---|---|---|---|
| chr6 | 17948403 | 17948415 | PKNOX2 | JASPAR | yes | 70328367 | ||
| chr6 | 17948403 | 17948415 | TGIF1 | JASPAR | yes | 70328368 | ||
| chr6 | 17948419 | 17948437 | MAFF | JASPAR | yes | 70328369 | ||
| chr6 | 17948421 | 17948436 | MAFK | JASPAR | yes | 70328370 | ||
| chr6 | 17948449 | 17948467 | NR3C1 | JASPAR | yes | 70328371 | ||
| chr6 | 17948476 | 17948480 | YY1 | TRANSFAC | yes | 70328372 | ||
| chr6 | 17948501 | 17948511 | ESX1 | JASPAR | yes | 70328373 | ||
| chr6 | 17948501 | 17948511 | RAX | JASPAR | yes | 70328374 | ||
| chr6 | 17948502 | 17948510 | BARX1 | JASPAR | yes | 70328375 | ||
| chr6 | 17948612 | 17948622 | NFATC3 | JASPAR | yes | 70328376 | ||
| chr6 | 17948614 | 17948621 | NFATC2 | JASPAR | yes | 70328377 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr6 | 17948461 | rs79754075 | T | C |
|
8880048 | |
| chr6 | 17948523 | rs562735808 | G | C | no | 8880049 | |
| chr6 | 17948535 | rs75126956 | A | C,G | no | 8880050 | |
| chr6 | 17948638 | rs12198586 | A | G | no | 8880051 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6 | 17759414 | 17987854 | - | KIF13A | ENSG00000137177.14 | 17987854 | 0.85 | 0.99 | 6185 | 60809 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|