| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100095979-100096413 | Common:3; Rare:136 | ||||
| chr7:100100039-100100271 | Common:1; Rare:113 | ||||
| chr7:100100299-100100558 | Common:3; Rare:90 | ||||
| chr7:100100630-100100898 | Common:2; Rare:113 | ||||
| chr7:100101253-100101723 | Common:1; Rare:191; Clinvar (benign):1 | ||||
| chr7:100119202-100119763 | Common:1; Rare:172; Clinvar:1 | ||||
| chr7:100127133-100127490 | Common:1; Rare:93 | ||||
| chr7:100148716-100149284 | Common:1; Rare:193 | ||||
| chr7:100158664-100158873 | Common:1; Rare:56 | ||||
| chr7:100177275-100177496 | Common:1; Rare:63 | ||||
| chr7:100177500-100177769 | Common:1; Rare:53 | ||||
| chr7:100272147-100272292 | Common:1; Rare:66 | ||||
| chr7:100367648-100367802 | Common:3; Rare:22 | ||||
| chr7:100428272-100428483 | Common:1; Rare:49 | ||||
| chr7:100428624-100428812 | Common:4; Rare:71 |