| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106112193-106112528 | Common:3; Rare:115 | ||||
| chr7:106284538-106284826 | Common:4; Rare:85 | ||||
| chr7:106284931-106285271 | Common:2; Rare:128 | ||||
| chr7:106660962-106661325 | Common:2; Rare:101 | ||||
| chr7:107044280-107044790 | Common:2; Rare:162 | ||||
| chr7:107168687-107169038 | Rare:117 | ||||
| chr7:107169664-107169970 | Common:3; Rare:92 | ||||
| chr7:107563867-107563996 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:107579990-107580360 | Common:4; Rare:124 | ||||
| chr7:107580380-107580800 | Common:3; Rare:116 | ||||
| chr7:107743556-107743790 | Common:3; Rare:83 | ||||
| chr7:107743964-107744172 | Common:1; Rare:59 | ||||
| chr7:107744350-107744750 | Common:3; Rare:107 | ||||
| chr7:107891004-107891194 | Rare:76 | ||||
| chr7:108003120-108003321 | Common:1; Rare:64 |