| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90245077-90245237 | Rare:49 | ||||
| chr7:90346553-90346769 | Common:4; Rare:94 | ||||
| chr7:90403312-90403553 | Common:1; Rare:60 | ||||
| chr7:91880650-91880827 | Common:2; Rare:51 | ||||
| chr7:91940735-91940993 | Common:4; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92134291-92134604 | Rare:101 | ||||
| chr7:92134716-92134898 | Common:3; Rare:56 | ||||
| chr7:92245837-92246006 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:92246099-92246482 | Common:3; Rare:144 | ||||
| chr7:92528364-92528822 | Common:4; Rare:140; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590009-92590151 | Rare:56 | ||||
| chr7:92833906-92834061 | Rare:39 | ||||
| chr7:92836216-92836509 | Rare:50 | ||||
| chr7:93117954-93118108 | Rare:27 | ||||
| chr7:93232173-93232417 | Common:2; Rare:55 |