Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22059600-22060340 | Common:5; Rare:183 | ||||
| chr8:22066760-22067170 | Common:3; Rare:145 | ||||
| chr8:22088870-22089435 | Common:31; Rare:784 | ||||
| chr8:22089366-22089900 | Common:11; Rare:433 | ||||
| chr8:22108917-22109317 | Common:6; Rare:113 | ||||
| chr8:22109278-22109616 | Common:26; Rare:458 | ||||
| chr8:22109561-22109961 | Common:12; Rare:252 | ||||
| chr8:22141030-22141564 | Common:4; Rare:262 | ||||
| chr8:22141790-22142160 | Common:9; Rare:200 | ||||
| chr8:22164467-22164730 | Common:2; Rare:67 | ||||
| chr8:22164710-22164960 | Common:3; Rare:51 | ||||
| chr8:22164901-22165896 | Common:17; Rare:525; Clinvar:3; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr8:22227220-22227540 | Common:7; Rare:181 | ||||
| chr8:22227649-22228077 | Common:8; Rare:345 | ||||
| chr8:22244227-22244627 | Common:4; Rare:76 |
- 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