| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100088889-100089036 | Common:1; Rare:50 | ||||
| chr7:100101306-100101723 | Common:1; Rare:166; Clinvar (benign):1 | ||||
| chr7:100119346-100119667 | Rare:92 | ||||
| chr7:100148716-100149042 | Common:1; Rare:143 | ||||
| chr7:100428637-100428786 | Common:2; Rare:58 | ||||
| chr7:100436452-100436644 | Rare:54 | ||||
| chr7:100479124-100479349 | Common:2; Rare:60 | ||||
| chr7:100612420-100612581 | Rare:31 | ||||
| chr7:100852590-100852762 | Common:1; Rare:43 | ||||
| chr7:100874955-100875209 | Common:2; Rare:86 | ||||
| chr7:101245055-101245172 | Common:1; Rare:41 | ||||
| chr7:101252292-101252527 | Common:1; Rare:49 | ||||
| chr7:101321707-101321880 | Common:3; Rare:59 | ||||
| chr7:101815649-101816051 | Common:1; Rare:111 | ||||
| chr7:102464848-102465023 | Rare:70 |