| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99558507-99558899 | Common:5; Rare:118 | ||||
| chr7:100081692-100081951 | Common:1; Rare:71 | ||||
| chr7:100101345-100101711 | Common:1; Rare:140; Clinvar (benign):1 | ||||
| chr7:100119335-100119667 | Rare:93 | ||||
| chr7:100373276-100373563 | Rare:50 | ||||
| chr7:100428636-100428804 | Common:4; Rare:65 | ||||
| chr7:100429138-100429453 | Common:4; Rare:145 | ||||
| chr7:100578435-100578712 | Rare:80 | ||||
| chr7:100586127-100586453 | Common:3; Rare:99 | ||||
| chr7:100673635-100673871 | Common:3; Rare:95 | ||||
| chr7:100852582-100852762 | Common:1; Rare:46 | ||||
| chr7:100874951-100875167 | Common:1; Rare:70 | ||||
| chr7:101217849-101218185 | Common:3; Rare:102 | ||||
| chr7:101815945-101816047 | Rare:33 | ||||
| chr7:102433363-102433583 | Common:2; Rare:58 |