| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94425757-94426052 | Rare:89; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94656049-94656380 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:95396354-95396508 | Common:2; Rare:66 | ||||
| chr7:95434929-95435147 | Common:1; Rare:104; Clinvar (benign):1 | ||||
| chr7:95596512-95596682 | Common:2; Rare:33 | ||||
| chr7:97117457-97117776 | Common:2; Rare:140 | ||||
| chr7:98252140-98252372 | Common:1; Rare:54 | ||||
| chr7:99325831-99325972 | Common:1; Rare:57 | ||||
| chr7:99408534-99408722 | Common:2; Rare:52 | ||||
| chr7:99408811-99409032 | Common:1; Rare:69 | ||||
| chr7:99438744-99438988 | Common:1; Rare:71 | ||||
| chr7:99472646-99472915 | Common:4; Rare:83 | ||||
| chr7:99500238-99500360 | Common:2; Rare:34 | ||||
| chr7:99558491-99558876 | Common:3; Rare:115 | ||||
| chr7:99679971-99680055 | Common:1; Rare:13 |