| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105014097-105014467 | Common:1; Rare:127 | ||||
| chr7:105268991-105269301 | Rare:51 | ||||
| chr7:105532055-105532256 | Common:3; Rare:50 | ||||
| chr7:105581459-105581552 | Rare:34 | ||||
| chr7:105876477-105876833 | Common:6; Rare:105 | ||||
| chr7:106112279-106112634 | Common:2; Rare:125 | ||||
| chr7:106284885-106285266 | Common:2; Rare:157 | ||||
| chr7:107469886-107470126 | Common:1; Rare:56 | ||||
| chr7:107563865-107564021 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107580091-107580306 | Common:2; Rare:79 | ||||
| chr7:107744053-107744184 | Rare:43 | ||||
| chr7:108003124-108003481 | Common:4; Rare:110 | ||||
| chr7:108526039-108526475 | Common:5; Rare:130 | ||||
| chr7:108569584-108569992 | Common:2; Rare:148 | ||||
| chr7:112206281-112206768 | Common:3; Rare:159 |