Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42540598-42540998 | Common:1; Rare:67 | ||||
| chr8:42540970-42541210 | Common:1; Rare:98 | ||||
| chr8:42541154-42541302 | Common:1; Rare:36 | ||||
| chr8:42541220-42542650 | Common:32; Rare:1428; Clinvar:13; Clinvar (benign):11 | ||||
| chr8:42842670-42843580 | Common:24; Rare:1061; Clinvar:27; Clinvar (benign):25; Clinvar (pathogenic):4 | ||||
| chr8:42896240-42896645 | Common:8; Rare:568 | ||||
| chr8:42896559-42897539 | Common:15; Rare:1486 | ||||
| chr8:43055500-43055980 | Common:3; Rare:169 | ||||
| chr8:43055981-43056805 | Common:10; Rare:1113 | ||||
| chr8:43056720-43056950 | Common:3; Rare:54 | ||||
| chr8:43093264-43093664 | Common:9; Rare:141; Clinvar (benign):3 | ||||
| chr8:43093813-43094213 | Common:4; Rare:162 | ||||
| chr8:43139860-43140781 | Common:20; Rare:831; Clinvar:30; Clinvar (benign):1 | ||||
| chr8:43140789-43141519 | Common:8; Rare:391 | ||||
| chr8:47260180-47260656 | Common:4; Rare:191 |
- 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