| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100604211-100604320 | Rare:29 | ||||
| chr7:100605630-100606020 | Common:2; Rare:187 | ||||
| chr7:100611926-100612210 | Common:6; Rare:104 | ||||
| chr7:100612366-100612601 | Rare:87 | ||||
| chr7:100632998-100633244 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100633250-100633476 | Rare:137; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:100673260-100673580 | Common:4; Rare:185 | ||||
| chr7:100673738-100673871 | Common:3; Rare:67 | ||||
| chr7:100705868-100706268 | Common:6; Rare:230 | ||||
| chr7:100827474-100827781 | Rare:208 | ||||
| chr7:100852572-100852786 | Common:3; Rare:104 | ||||
| chr7:100867194-100867587 | Common:8; Rare:241 | ||||
| chr7:100874927-100875243 | Common:4; Rare:209 | ||||
| chr7:100884150-100884600 | Common:4; Rare:171 | ||||
| chr7:100889628-100889912 | Common:14; Rare:179 |