| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:103149233-103149372 | Common:2; Rare:36 | ||||
| chr7:103344696-103345123 | Common:2; Rare:104 | ||||
| chr7:104207961-104208112 | Common:3; Rare:69 | ||||
| chr7:105013585-105013712 | Common:1; Rare:44 | ||||
| chr7:105014087-105014269 | Common:1; Rare:73 | ||||
| chr7:105108777-105109083 | Rare:71 | ||||
| chr7:105532055-105532279 | Common:3; Rare:60 | ||||
| chr7:105581469-105581631 | Rare:49 | ||||
| chr7:105876470-105876829 | Common:6; Rare:105 | ||||
| chr7:106112208-106112490 | Common:3; Rare:94 | ||||
| chr7:106284973-106285443 | Common:6; Rare:164 | ||||
| chr7:106285539-106285639 | Rare:26 | ||||
| chr7:107168705-107169014 | Rare:100 | ||||
| chr7:107563861-107564037 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580147-107580278 | Common:2; Rare:53 |