Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137077098-137077546 | Common:8; Rare:344 | ||||
| chr9:137085807-137086529 | Common:4; Rare:167 | ||||
| chr9:137086542-137087171 | Common:10; Rare:1228; Clinvar:32; Clinvar (benign):6 | ||||
| chr9:137087172-137087958 | Common:8; Rare:528; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:137113031-137113964 | Common:7; Rare:502 | ||||
| chr9:137114215-137115454 | Common:10; Rare:1026 | ||||
| chr9:137156950-137157301 | Common:4; Rare:355; Clinvar:4; Clinvar (benign):8 | ||||
| chr9:137163098-137163498 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):18 | ||||
| chr9:137168040-137168450 | Rare:110 | ||||
| chr9:137188499-137189494 | Common:20; Rare:1509 | ||||
| chr9:137200072-137200550 | Common:4; Rare:180; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr9:137200635-137201189 | Common:12; Rare:520 | ||||
| chr9:137205440-137205910 | Common:6; Rare:698 | ||||
| chr9:137223869-137224269 | Common:2; Rare:98 | ||||
| chr9:137224917-137225324 | Common:6; Rare:241 |
- 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