Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:146144233-146144841 | Common:2; Rare:256; Clinvar:2; Clinvar (benign):9 | ||||
| chr5:146182392-146182967 | Common:24; Rare:760 | ||||
| chr5:146203165-146204084 | Common:14; Rare:644 | ||||
| chr5:146446852-146448271 | Common:33; Rare:1207 | ||||
| chr5:148320300-148320853 | Common:19; Rare:274 | ||||
| chr5:148383560-148384150 | Common:1; Rare:663 | ||||
| chr5:149062358-149063520 | Common:11; Rare:416; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr5:149141257-149141784 | Common:3; Rare:281 | ||||
| chr5:149345134-149345682 | Common:11; Rare:730 | ||||
| chr5:149357435-149358103 | Common:29; Rare:389 | ||||
| chr5:149549623-149551112 | Common:7; Rare:663 | ||||
| chr5:149551310-149552091 | Common:8; Rare:876 | ||||
| chr5:149729770-149730393 | Common:9; Rare:578 | ||||
| chr5:149960069-149960469 | Common:3; Rare:104 | ||||
| chr5:149960457-149960918 | Common:7; Rare:697; Clinvar:34 |
- 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