| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100586093-100586456 | Common:6; Rare:232 | ||||
| chr7:100602177-100602419 | Common:2; Rare:94 | ||||
| chr7:100611932-100612206 | Common:8; Rare:110 | ||||
| chr7:100612395-100612606 | Rare:74 | ||||
| chr7:100632918-100633816 | Common:2; Rare:512; Clinvar:17; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr7:100641560-100642090 | Common:2; Rare:195 | ||||
| chr7:100642702-100642826 | Rare:28 | ||||
| chr7:100673270-100673560 | Common:3; Rare:166 | ||||
| chr7:100673736-100673913 | Common:8; Rare:160 | ||||
| chr7:100705897-100706268 | Common:8; Rare:242 | ||||
| chr7:100720920-100721273 | Rare:125 | ||||
| chr7:100827403-100827873 | Common:2; Rare:285 | ||||
| chr7:100852569-100852786 | Common:4; Rare:107 | ||||
| chr7:100874918-100875247 | Common:4; Rare:213 | ||||
| chr7:100889628-100889902 | Common:13; Rare:171 |