Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30786778-30787092 | Rare:70 | ||||
| chr16:30787173-30787512 | Common:1; Rare:70 | ||||
| chr16:30893996-30894328 | Common:5; Rare:80 | ||||
| chr16:30896330-30896940 | Common:2; Rare:126 | ||||
| chr16:30896985-30897381 | Common:1; Rare:62 | ||||
| chr16:30922478-30922904 | Common:2; Rare:120 | ||||
| chr16:30923161-30923614 | Common:1; Rare:122 | ||||
| chr16:30957067-30957340 | Common:3; Rare:56 | ||||
| chr16:30957559-30957787 | Common:1; Rare:66 | ||||
| chr16:30996609-30996730 | Rare:23; Clinvar (benign):1 | ||||
| chr16:30997258-30997432 | Common:1; Rare:39 | ||||
| chr16:31033391-31033611 | Common:1; Rare:81 | ||||
| chr16:31073456-31073876 | Rare:113 | ||||
| chr16:31074153-31074473 | Common:2; Rare:92 | ||||
| chr16:31094643-31095040 | Common:1; Rare:122; Clinvar:1; 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