| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99438713-99439038 | Common:2; Rare:101 | ||||
| chr7:99472659-99472967 | Common:4; Rare:96 | ||||
| chr7:99500216-99500424 | Common:3; Rare:56 | ||||
| chr7:99558519-99558917 | Common:5; Rare:116 | ||||
| chr7:100049695-100049823 | Rare:48 | ||||
| chr7:100081692-100081991 | Common:2; Rare:79 | ||||
| chr7:100082553-100082858 | Rare:54 | ||||
| chr7:100088895-100089057 | Common:1; Rare:54 | ||||
| chr7:100101333-100101706 | Common:1; Rare:144; Clinvar (benign):1 | ||||
| chr7:100119335-100119728 | Rare:118 | ||||
| chr7:100122537-100122847 | Common:1; Rare:79 | ||||
| chr7:100148856-100149046 | Rare:103 | ||||
| chr7:100428603-100428824 | Common:5; Rare:86 | ||||
| chr7:100429137-100429449 | Common:4; Rare:144 | ||||
| chr7:100611984-100612185 | Common:2; Rare:42 |