Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34665851-34666260 | Common:12; Rare:321 | ||||
| chr9:34989090-34989951 | Common:6; Rare:372 | ||||
| chr9:34989985-34990385 | Common:2; Rare:203 | ||||
| chr9:34992311-34992774 | Common:9; Rare:212 | ||||
| chr9:35071810-35072367 | Common:4; Rare:537 | ||||
| chr9:35072521-35073017 | Rare:357; Clinvar:12; Clinvar (benign):4 | ||||
| chr9:35078725-35079549 | Common:4; Rare:297; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr9:35079454-35079871 | Rare:211; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:35079880-35080370 | Common:26; Rare:382; Clinvar:15; Clinvar (benign):18 | ||||
| chr9:35095410-35096866 | Common:7; Rare:773; Clinvar:12; Clinvar (benign):4 | ||||
| chr9:35101159-35101750 | Common:5; Rare:288 | ||||
| chr9:35102289-35102813 | Common:1; Rare:146 | ||||
| chr9:35103013-35103413 | Common:6; Rare:552 | ||||
| chr9:35110903-35111452 | Rare:285 | ||||
| chr9:35111470-35112209 | Common:5; Rare:421 |
- 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