| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87876224-87876648 | Common:2; Rare:181 | ||||
| chr7:88306835-88306942 | Rare:28 | ||||
| chr7:90211633-90211934 | Common:4; Rare:94 | ||||
| chr7:90245095-90245243 | Rare:51 | ||||
| chr7:90346595-90346736 | Common:3; Rare:59 | ||||
| chr7:90403458-90403518 | Rare:20 | ||||
| chr7:91880668-91880801 | Common:1; Rare:36 | ||||
| chr7:91940755-91941004 | Common:4; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134372-92134570 | Rare:62 | ||||
| chr7:92134721-92134838 | Common:3; Rare:28 | ||||
| chr7:92245865-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246109-92246430 | Common:3; Rare:111 | ||||
| chr7:92528389-92528816 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:94004317-94004435 | Rare:42 | ||||
| chr7:94394543-94394937 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 |