Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49018312-49018459 | Common:1; Rare:47 | ||||
| chr3:49018564-49018683 | Common:1; Rare:43 | ||||
| chr3:49020674-49020821 | Common:1; Rare:41 | ||||
| chr3:49021417-49021768 | Common:1; Rare:87; Clinvar:1 | ||||
| chr3:49021897-49022208 | Rare:96; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr3:49029374-49029605 | Common:2; Rare:156 | ||||
| chr3:49093571-49093790 | Common:1; Rare:71 | ||||
| chr3:49093987-49094204 | Rare:50 | ||||
| chr3:49094324-49094702 | Common:2; Rare:100 | ||||
| chr3:49104689-49105014 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49120735-49120960 | Rare:70 | ||||
| chr3:49132243-49132643 | Common:1; Rare:187; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:49132988-49133333 | Rare:63; Clinvar:1 | ||||
| chr3:49166280-49166521 | Common:1; Rare:55 | ||||
| chr3:49171450-49171638 | Common:2; Rare:39 |
- 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