| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100148716-100149017 | Common:1; Rare:131 | ||||
| chr7:100428636-100428793 | Common:3; Rare:60 | ||||
| chr7:100852619-100852762 | Rare:37 | ||||
| chr7:100874870-100875202 | Common:1; Rare:117 | ||||
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:102464852-102465014 | Rare:67 | ||||
| chr7:104207943-104208112 | Common:3; Rare:85 | ||||
| chr7:105014055-105014249 | Common:2; Rare:83 | ||||
| chr7:105532078-105532240 | Common:1; Rare:43 | ||||
| chr7:105876481-105876829 | Common:6; Rare:104 | ||||
| chr7:106284849-106285441 | Common:6; Rare:218 | ||||
| chr7:106285539-106285592 | Rare:14 | ||||
| chr7:107563879-107563996 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:107580162-107580294 | Common:2; Rare:54 | ||||
| chr7:107744053-107744159 | Rare:36 |