| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:135148028-135148158 | Rare:34 | ||||
| chr7:139036014-139036208 | Rare:53 | ||||
| chr7:141738043-141738396 | Common:4; Rare:106 | ||||
| chr7:143380961-143381391 | Common:1; Rare:143 | ||||
| chr7:148698774-148698965 | Common:1; Rare:67 | ||||
| chr7:149147292-149147482 | Common:3; Rare:48 | ||||
| chr7:149873802-149874038 | Common:3; Rare:94 | ||||
| chr7:151227153-151227406 | Common:1; Rare:72 | ||||
| chr7:151341810-151341845 | Rare:7 | ||||
| chr7:156640556-156640689 | Common:2; Rare:72 | ||||
| chr7:157336750-157337016 | Common:1; Rare:113 | ||||
| chr8:6406521-6406667 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:11769565-11769788 | Common:5; Rare:98 | ||||
| chr8:17246804-17247006 | Common:2; Rare:86 | ||||
| chr8:23854548-23854595 | Rare:19 |