| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27740022-27740268 | Common:6; Rare:81 | ||||
| chr7:27828448-27828772 | Rare:74 | ||||
| chr7:28412434-28412515 | Rare:21 | ||||
| chr7:28685802-28686166 | Common:2; Rare:88 | ||||
| chr7:29194719-29194938 | Common:2; Rare:54 | ||||
| chr7:29989722-29989922 | Rare:81 | ||||
| chr7:30026574-30026989 | Common:1; Rare:98 | ||||
| chr7:30028204-30028392 | Rare:61 | ||||
| chr7:30135184-30135248 | Rare:19 | ||||
| chr7:30146107-30146257 | Rare:44 | ||||
| chr7:30478681-30478825 | Common:1; Rare:53 | ||||
| chr7:30504712-30505126 | Common:4; Rare:139 | ||||
| chr7:30549998-30550271 | Common:1; Rare:47 | ||||
| chr7:30551084-30551316 | Rare:50 | ||||
| chr7:30594660-30595136 | Common:9; Rare:198; Clinvar:11; Clinvar (benign):18 |