| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1570024-1570102 | Common:1; Rare:25 | ||||
| chr7:2242177-2242255 | Common:2; Rare:45 | ||||
| chr7:5513746-5513855 | Common:1; Rare:52 | ||||
| chr7:6009029-6009323 | Common:3; Rare:123; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:6401722-6401978 | Rare:51 | ||||
| chr7:6706945-6707085 | Rare:56 | ||||
| chr7:12211136-12211399 | Common:3; Rare:120 | ||||
| chr7:12687470-12687643 | Common:5; Rare:43 | ||||
| chr7:15686549-15686738 | Common:2; Rare:54 | ||||
| chr7:16645690-16646211 | Common:4; Rare:184 | ||||
| chr7:17940454-17940540 | Common:1; Rare:45 | ||||
| chr7:20331760-20331854 | Common:1; Rare:35 | ||||
| chr7:23181954-23182064 | Rare:44 | ||||
| chr7:23470358-23470557 | Rare:60 | ||||
| chr7:23531954-23532105 | Common:1; Rare:59 |