Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:38392438-38393190 | Common:13; Rare:598 | ||||
| chr9:42129340-42129700 | Common:2; Rare:59 | ||||
| chr9:65675633-65676033 | Common:3; Rare:249 | ||||
| chr9:66900533-66901374 | Common:10; Rare:329 | ||||
| chr9:68704876-68705281 | Common:3; Rare:259 | ||||
| chr9:68705301-68705804 | Common:13; Rare:468 | ||||
| chr9:68705746-68706239 | Common:3; Rare:172 | ||||
| chr9:68706258-68706724 | Common:2; Rare:162 | ||||
| chr9:68779331-68779731 | Rare:65 | ||||
| chr9:68779740-68780528 | Common:27; Rare:818 | ||||
| chr9:69035470-69035820 | Common:3; Rare:100; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:69035840-69036270 | Common:9; Rare:375; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr9:69036418-69036818 | Common:3; Rare:119 | ||||
| chr9:69173638-69175460 | Common:50; Rare:1183; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:69759310-69759860 | Common:8; Rare:296 |
- 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