Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98577086-98577263 | Common:1; Rare:49 | ||||
| chr13:98752656-98752906 | Common:3; Rare:61 | ||||
| chr13:99086610-99086804 | Common:2; Rare:79 | ||||
| chr13:99200603-99200946 | Common:7; Rare:147 | ||||
| chr13:99314790-99315092 | Rare:65 | ||||
| chr13:99501212-99501524 | Common:1; Rare:96 | ||||
| chr13:99606487-99606827 | Common:5; Rare:132 | ||||
| chr13:99606942-99607082 | Common:3; Rare:30 | ||||
| chr13:99981306-99981410 | Rare:33 | ||||
| chr13:99981569-99981782 | Common:1; Rare:75 | ||||
| chr13:99982131-99982930 | Common:2; Rare:314; Clinvar:2; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr13:100088834-100089160 | Rare:132; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:100588550-100589100 | Common:6; Rare:152 | ||||
| chr13:100674690-100675369 | Common:7; Rare:264 | ||||
| chr13:102596760-102597039 | Common:1; Rare:125 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box