Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58007135-58007454 | Common:1; Rare:152 | ||||
| chr17:58007546-58007814 | Common:1; Rare:59 | ||||
| chr17:58083158-58083471 | Common:4; Rare:118 | ||||
| chr17:58219185-58219406 | Common:1; Rare:84; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:58352123-58352496 | Common:6; Rare:140 | ||||
| chr17:58353059-58353216 | Common:1; Rare:32 | ||||
| chr17:58415494-58415939 | Rare:107 | ||||
| chr17:58417455-58417845 | Common:1; Rare:74 | ||||
| chr17:58514002-58514144 | Rare:27 | ||||
| chr17:58514581-58514793 | Rare:45 | ||||
| chr17:58517835-58518361 | Common:1; Rare:118 | ||||
| chr17:58531981-58532148 | Rare:41 | ||||
| chr17:58692501-58692783 | Common:3; Rare:145; Clinvar:33; Clinvar (benign):29; Clinvar (pathogenic):2 | ||||
| chr17:58692810-58693060 | Common:1; Rare:60 | ||||
| chr17:59106681-59107250 | Common:3; Rare:181; Clinvar:5; Clinvar (benign):4 |
- 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