| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101019909-101020216 | Common:2; Rare:88 | ||||
| chr7:101165567-101165651 | Rare:26 | ||||
| chr7:101200883-101201169 | Common:1; Rare:51 | ||||
| chr7:101210547-101210822 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:101240389-101240693 | Common:2; Rare:71 | ||||
| chr7:101241025-101241335 | Common:1; Rare:54 | ||||
| chr7:101244984-101245172 | Common:1; Rare:81 | ||||
| chr7:102464844-102465014 | Common:1; Rare:69 | ||||
| chr7:102748696-102749035 | Common:2; Rare:79 | ||||
| chr7:103149045-103149389 | Common:6; Rare:99 | ||||
| chr7:103149469-103149651 | Rare:47 | ||||
| chr7:103344561-103344584 | Rare:6 | ||||
| chr7:104207973-104208112 | Common:2; Rare:59 | ||||
| chr7:105014028-105014291 | Common:3; Rare:99 |