Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34329150-34329832 | Common:8; Rare:1016 | ||||
| chr9:34376777-34377256 | Common:3; Rare:257 | ||||
| chr9:34380651-34381051 | Common:2; Rare:144 | ||||
| chr9:34458471-34458871 | Common:7; Rare:419; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:34522940-34523330 | Common:2; Rare:124 | ||||
| chr9:34611997-34612397 | Common:42; Rare:389 | ||||
| chr9:34620380-34620690 | Common:4; Rare:197 | ||||
| chr9:34637470-34638250 | Common:14; Rare:695; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:34646369-34646800 | Common:4; Rare:315; Clinvar:12; Clinvar (pathogenic):5 | ||||
| chr9:34646800-34647260 | Rare:208; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):18 | ||||
| chr9:34647511-34648027 | Common:4; Rare:240; Clinvar:22; Clinvar (benign):11; Clinvar (pathogenic):65 | ||||
| chr9:34651910-34652368 | Common:1; Rare:445 | ||||
| chr9:34662988-34663388 | Common:3; Rare:113 | ||||
| chr9:34664251-34664651 | Common:5; Rare:79 | ||||
| chr9:34665286-34665690 | Rare:709 |
- 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