| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88220011-88220151 | Rare:69 | ||||
| chr7:88306873-88307002 | Rare:25 | ||||
| chr7:90211589-90211953 | Common:4; Rare:109 | ||||
| chr7:90245095-90245243 | Rare:51 | ||||
| chr7:90346589-90346738 | Common:4; Rare:61 | ||||
| chr7:90403163-90403529 | Common:2; Rare:82 | ||||
| chr7:90595867-90596048 | Common:6; Rare:70 | ||||
| chr7:90596222-90596484 | Rare:85 | ||||
| chr7:91880672-91880801 | Common:1; Rare:35 | ||||
| chr7:91940830-91941004 | Common:3; Rare:59; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134434-92134604 | Rare:52 | ||||
| chr7:92134779-92134883 | Common:2; Rare:34 | ||||
| chr7:92245848-92246269 | Common:6; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528370-92528822 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833902-92834007 | Rare:28 |