Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128343295-128344200 | Common:15; Rare:506 | ||||
| chr7:128361480-128362010 | Common:4; Rare:121 | ||||
| chr7:128405837-128406237 | Common:11; Rare:419 | ||||
| chr7:128409370-128409811 | Common:8; Rare:255; Clinvar:6 | ||||
| chr7:128409770-128409880 | Rare:39; Clinvar:1 | ||||
| chr7:128409816-128410140 | Common:5; Rare:338; Clinvar:7; Clinvar (benign):5 | ||||
| chr7:128410150-128410680 | Common:11; Rare:210 | ||||
| chr7:128455460-128456120 | Common:18; Rare:829 | ||||
| chr7:128476499-128476904 | Common:11; Rare:679 | ||||
| chr7:128738679-128738938 | Rare:58 | ||||
| chr7:128738987-128739555 | Common:17; Rare:717 | ||||
| chr7:128739563-128740180 | Common:9; Rare:236 | ||||
| chr7:128791150-128791560 | Common:8; Rare:434 | ||||
| chr7:128829641-128830923 | Common:32; Rare:1047; Clinvar:18; Clinvar (benign):9 | ||||
| chr7:128830854-128831228 | Common:1; Rare:107; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 |
- 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