| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100867059-100867167 | Rare:22 | ||||
| chr7:100867169-100867201 | Rare:6 | ||||
| chr7:100867211-100867457 | Common:3; Rare:73 | ||||
| chr7:100874942-100875255 | Common:2; Rare:106 | ||||
| chr7:100889650-100889871 | Common:6; Rare:71 | ||||
| chr7:101085352-101085711 | Common:2; Rare:63 | ||||
| chr7:101126968-101127122 | Common:1; Rare:30 | ||||
| chr7:101154336-101154512 | Common:1; Rare:66 | ||||
| chr7:101165543-101165642 | Rare:30 | ||||
| chr7:101210091-101210335 | Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:101217847-101218195 | Common:4; Rare:109 | ||||
| chr7:101244988-101245178 | Common:1; Rare:80 | ||||
| chr7:101252282-101252516 | Common:1; Rare:51 | ||||
| chr7:101321700-101321881 | Common:3; Rare:62 | ||||
| chr7:101815573-101816033 | Common:3; Rare:132 |