| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106285917-106286058 | Rare:29 | ||||
| chr7:106661017-106661081 | Rare:21 | ||||
| chr7:106661122-106661293 | Common:1; Rare:32 | ||||
| chr7:107563831-107564088 | Common:2; Rare:136; Clinvar:2; Clinvar (benign):6 | ||||
| chr7:107564327-107564603 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:107580123-107580555 | Common:4; Rare:140 | ||||
| chr7:107660490-107660675 | Common:1; Rare:47; Clinvar:2 | ||||
| chr7:107660678-107660802 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:107660810-107661178 | Common:3; Rare:73; Clinvar (pathogenic):1 | ||||
| chr7:107661290-107661519 | Common:2; Rare:54 | ||||
| chr7:107693022-107693054 | Rare:6 | ||||
| chr7:107743582-107743806 | Common:3; Rare:87 | ||||
| chr7:107744016-107744171 | Rare:47 | ||||
| chr7:107929081-107929817 | Common:4; Rare:191; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:108002070-108002198 | Common:2; Rare:38 |