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 |
|---|---|---|---|---|---|---|---|---|
| chr2 | 74722840 | 74722854 | STAT1 | JASPAR | yes | 22083727 | ||
| chr2 | 74722871 | 74722888 | BCL6B | JASPAR | yes | 22083728 | ||
| chr2 | 74722872 | 74722887 | STAT1 | JASPAR | yes | 22083729 | ||
| chr2 | 74722874 | 74722885 | STAT1 | JASPAR | yes | 22083730 | ||
| chr2 | 74722874 | 74722885 | STAT3 | JASPAR | yes | 22083731 | ||
| chr2 | 74722914 | 74722924 | NFIA | JASPAR | yes | 22083732 | ||
| chr2 | 74722916 | 74722922 | NFIC | JASPAR | yes | 22083733 | ||
| chr2 | 74722924 | 74722934 | NFATC3 | JASPAR | yes | 22083734 | ||
| chr2 | 74722926 | 74722933 | NFATC2 | JASPAR | yes | 22083735 | ||
| chr2 | 74722937 | 74722941 | LFA1 | TRANSFAC | yes | 22083736 | ||
| chr2 | 74722962 | 74722978 | SOX4 | JASPAR | yes | 22083737 | ||
| chr2 | 74722969 | 74722984 | HSF1 | JASPAR | yes | 22083738 | ||
| chr2 | 74722970 | 74722983 | HSF2 | JASPAR | yes | 22083739 | ||
| chr2 | 74722989 | 74722993 | YY1 | TRANSFAC | yes | 22083740 | ||
| chr2 | 74723011 | 74723015 | LFA1 | TRANSFAC | yes | 22083741 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr2 | 74722867 | rs148717736 | A | C | no | 5852475 | |
| chr2 | 74722873 | rs189531883 | G | T |
|
5852476 |
| 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 | 74641304 | 74648718 | - | C2orf81 | ENSG00000159239.7 | 74648718 | 0.78 | 1.0 | 2484 | 25883 | |
| chr2 | 74648805 | 74652882 | + | WDR54 | ENSG00000005448.12 | 74648805 | 0.84 | 1.0 | 2485 | 25970 | |
| chr2 | 74652963 | 74669549 | - | RTKN | ENSG00000114993.11 | 74669549 | 0.86 | 1.0 | 2486 | 46714 | |
| chr2 | 74682150 | 74688011 | + | INO80B | ENSG00000115274.10 | 74682150 | 0.69 | 0.99 | 2487 | 59315 | |
| chr2 | 74685456 | 74688018 | + | WBP1 | ENSG00000239779.2 | 74685456 | 0.68 | 0.98 | 2488 | 62621 | |
| chr2 | 74688184 | 74692537 | - | MOGS | ENSG00000115275.7 | 74692537 | 0.55 | 1.0 | 2489 | 69702 | |
| chr2 | 74699085 | 74700449 | - | MRPL53 | ENSG00000204822.6 | 74700449 | 0.87 | 0.76 | 2490 | 77614 | |
| chr2 | 74699113 | 74710535 | - | CCDC142 | ENSG00000135637.9 | 74710535 | 0.59 | 1.0 | 2491 | 87700 | |
| chr2 | 74710200 | 74722013 | + | TTC31 | ENSG00000115282.15 | 74710200 | 0.54 | 1.0 | 2492 | 87365 | |
| chr2 | 74724644 | 74730443 | - | LBX2 | ENSG00000179528.11 | 74730443 | 0.92 | 1.0 | 2493 | 92578 | |
| chr2 | 74732170 | 74735707 | - | PCGF1 | ENSG00000115289.8 | 74735707 | 0.67 | 1.0 | 2494 | 87314 | |
| chr2 | 74740590 | 74744274 | + | TLX2 | ENSG00000115297.9 | 74740590 | 0.97 | 0.95 | 2495 | 82431 | |
| chr2 | 74745258 | 74753463 | - | DQX1 | ENSG00000144045.9 | 74753463 | 0.94 | 0.97 | 2496 | 69558 | |
| chr2 | 74753772 | 74757066 | - | AUP1 | ENSG00000115307.12 | 74757066 | 0.56 | 1.0 | 2497 | 65955 | |
| chr2 | 74756504 | 74760472 | + | HTRA2 | ENSG00000115317.7 | 74756504 | 0.51 | 1.0 | 2498 | 66517 | |
| chr2 | 74759541 | 74782817 | - | LOXL3 | ENSG00000115318.7 | 74782817 | 0.81 | 1.0 | 2499 | 40204 | |
| chr2 | 74776153 | 74784681 | + | DOK1 | ENSG00000115325.9 | 74776153 | 0.88 | 1.0 | 2500 | 46868 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|