| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100100493-100100852 | Common:1; Rare:148 | ||||
| chr7:100101343-100101707 | Common:1; Rare:137; Clinvar (benign):1 | ||||
| chr7:100119302-100119671 | Rare:109 | ||||
| chr7:100352124-100352347 | Common:2; Rare:36 | ||||
| chr7:100428636-100428795 | Common:3; Rare:60 | ||||
| chr7:100428817-100428918 | Rare:44 | ||||
| chr7:100436152-100436225 | Common:1; Rare:20 | ||||
| chr7:100436449-100436796 | Rare:104 | ||||
| chr7:100586116-100586456 | Common:3; Rare:109 | ||||
| chr7:100604205-100604446 | Common:1; Rare:58 | ||||
| chr7:100612407-100612581 | Rare:34 | ||||
| chr7:100687585-100687739 | Rare:43 | ||||
| chr7:100852612-100852747 | Rare:35 | ||||
| chr7:100867266-100867425 | Rare:47 | ||||
| chr7:100874934-100875296 | Common:2; Rare:121 |