| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94656122-94656380 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:97117459-97117711 | Common:1; Rare:96 | ||||
| chr7:99325805-99325946 | Common:1; Rare:55 | ||||
| chr7:99408547-99409009 | Common:3; Rare:134 | ||||
| chr7:99438727-99438985 | Common:1; Rare:79 | ||||
| chr7:99500265-99500417 | Common:1; Rare:41 | ||||
| chr7:99558519-99558880 | Common:3; Rare:105 | ||||
| chr7:100101327-100101684 | Common:1; Rare:135 | ||||
| chr7:100119341-100119742 | Rare:121; Clinvar:1 | ||||
| chr7:100428643-100428809 | Common:4; Rare:62 | ||||
| chr7:100603069-100603172 | Rare:14 | ||||
| chr7:100604824-100605112 | Rare:73 | ||||
| chr7:100705887-100706165 | Common:2; Rare:102 | ||||
| chr7:100867211-100867425 | Common:1; Rare:64 | ||||
| chr7:100874951-100875202 | Common:1; Rare:83 |