| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107469994-107470274 | Rare:64 | ||||
| chr7:107563879-107564022 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107580160-107580459 | Common:3; Rare:106 | ||||
| chr7:107743614-107743801 | Common:3; Rare:70 | ||||
| chr7:107744066-107744205 | Rare:50 | ||||
| chr7:107891022-107891252 | Rare:107; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:108456663-108456751 | Rare:24 | ||||
| chr7:108526032-108526475 | Common:5; Rare:130 | ||||
| chr7:108569572-108570056 | Common:3; Rare:172 | ||||
| chr7:111090935-111091270 | Rare:65 | ||||
| chr7:111091337-111091502 | Rare:29 | ||||
| chr7:112206297-112206789 | Common:2; Rare:165 | ||||
| chr7:112450176-112450496 | Common:6; Rare:96 | ||||
| chr7:112790164-112790451 | Common:1; Rare:79 | ||||
| chr7:112939645-112940178 | Common:4; Rare:171 |