| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90709558-90709939 | Common:4; Rare:72 | ||||
| chr7:91940729-91940989 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92134442-92134604 | Rare:50 | ||||
| chr7:92134734-92134898 | Common:3; Rare:47 | ||||
| chr7:92528336-92528816 | Common:3; Rare:146; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833905-92834024 | Rare:31 | ||||
| chr7:93148351-93148404 | Rare:9 | ||||
| chr7:93232201-93232395 | Common:2; Rare:34 | ||||
| chr7:93921988-93922088 | Common:2; Rare:24 | ||||
| chr7:94004310-94004506 | Rare:56 | ||||
| chr7:94509791-94510106 | Rare:107 | ||||
| chr7:94656122-94656381 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:97117484-97117759 | Common:1; Rare:115 | ||||
| chr7:97872090-97872224 | Rare:44 | ||||
| chr7:97872389-97872577 | Common:2; Rare:60 |