| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:95434882-95435113 | Common:1; Rare:98; Clinvar (benign):1 | ||||
| chr7:96322018-96322214 | Rare:87; Clinvar:4 | ||||
| chr7:96709689-96709899 | Common:1; Rare:77 | ||||
| chr7:97869121-97869370 | Common:3; Rare:41; Clinvar (pathogenic):1 | ||||
| chr7:98246118-98246223 | Common:1; Rare:32 | ||||
| chr7:98252125-98252400 | Common:2; Rare:64 | ||||
| chr7:98281839-98281952 | Common:1; Rare:30 | ||||
| chr7:98282122-98282451 | Common:2; Rare:114 | ||||
| chr7:99325801-99325997 | Common:1; Rare:77 | ||||
| chr7:99404668-99404792 | Common:1; Rare:29 | ||||
| chr7:99408537-99408729 | Common:2; Rare:54 | ||||
| chr7:99408737-99409239 | Common:2; Rare:141 | ||||
| chr7:99438708-99439109 | Common:3; Rare:121 | ||||
| chr7:99439250-99439470 | Common:2; Rare:53 | ||||
| chr7:99466116-99466258 | Rare:52 |