| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:15686808-15686848 | Rare:16 | ||||
| chr7:16645646-16646213 | Common:4; Rare:195 | ||||
| chr7:17940411-17940582 | Common:1; Rare:89 | ||||
| chr7:18086692-18087068 | Common:5; Rare:146 | ||||
| chr7:20330842-20330918 | Rare:17 | ||||
| chr7:20331721-20331865 | Common:1; Rare:51 | ||||
| chr7:21427839-21428146 | Common:1; Rare:112 | ||||
| chr7:22726986-22727205 | Common:1; Rare:24 | ||||
| chr7:23105678-23105967 | Common:2; Rare:132; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181757-23182107 | Common:2; Rare:129 | ||||
| chr7:23531928-23532106 | Common:2; Rare:73 | ||||
| chr7:24980113-24980360 | Common:6; Rare:102 | ||||
| chr7:25125202-25125643 | Rare:180; Clinvar:3 | ||||
| chr7:25180088-25180146 | Rare:19 | ||||
| chr7:26200573-26201008 | Common:2; Rare:211 |