Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50909672-50909816 | Rare:30; Clinvar:2 | ||||
| chr13:50909989-50910376 | Common:2; Rare:107; Clinvar:1 | ||||
| chr13:51222126-51222412 | Common:3; Rare:92 | ||||
| chr13:51451526-51451708 | Rare:51 | ||||
| chr13:51452988-51453462 | Common:1; Rare:185 | ||||
| chr13:51453612-51453729 | Common:2; Rare:33 | ||||
| chr13:51453985-51454385 | Common:1; Rare:132 | ||||
| chr13:51583979-51584194 | Common:1; Rare:59 | ||||
| chr13:51584233-51584534 | Common:3; Rare:102 | ||||
| chr13:51584824-51584998 | Common:1; Rare:51 | ||||
| chr13:51803681-51803888 | Rare:59 | ||||
| chr13:51804107-51804315 | Common:2; Rare:58 | ||||
| chr13:51978975-51979375 | Common:3; Rare:102 | ||||
| chr13:52011686-52011801 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr13:52012006-52012490 | Common:2; Rare:177; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |
- 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