| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23470452-23470539 | Rare:25 | ||||
| chr7:23531958-23532083 | Common:1; Rare:50 | ||||
| chr7:24980176-24980414 | Common:8; Rare:104 | ||||
| chr7:25125275-25125643 | Rare:138; Clinvar:2 | ||||
| chr7:26201323-26201805 | Common:2; Rare:217 | ||||
| chr7:27740083-27740199 | Common:3; Rare:30 | ||||
| chr7:30504762-30505090 | Common:2; Rare:108 | ||||
| chr7:30594733-30594927 | Common:2; Rare:90; Clinvar:5; Clinvar (benign):5 | ||||
| chr7:30771324-30771445 | Common:1; Rare:35 | ||||
| chr7:32490319-32490468 | Common:1; Rare:50 | ||||
| chr7:32495238-32495557 | Rare:82 | ||||
| chr7:33062732-33062905 | Common:3; Rare:76 | ||||
| chr7:35800945-35801252 | Common:2; Rare:130 | ||||
| chr7:38177996-38178397 | Common:4; Rare:122 | ||||
| chr7:39012992-39013170 | Rare:51 |