| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139109343-139109487 | Common:1; Rare:44 | ||||
| chr7:139359648-139359968 | Common:2; Rare:136 | ||||
| chr7:151080796-151080979 | Rare:60 | ||||
| chr7:155644384-155644697 | Common:2; Rare:99 | ||||
| chr7:157336770-157337085 | Common:2; Rare:152; Clinvar:2 | ||||
| chr8:232217-232377 | Common:2; Rare:63 | ||||
| chr8:6406533-6406668 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:11802461-11802810 | Common:6; Rare:190 | ||||
| chr8:17246826-17246982 | Common:1; Rare:63 | ||||
| chr8:22245024-22245444 | Common:2; Rare:150 | ||||
| chr8:22669093-22669241 | Common:2; Rare:52 | ||||
| chr8:23457624-23457771 | Common:2; Rare:58 | ||||
| chr8:25458221-25458608 | Common:2; Rare:108 | ||||
| chr8:26382991-26383099 | Rare:55 | ||||
| chr8:30156228-30156379 | Common:1; Rare:45 |