| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39584045-39584422 | Common:1; Rare:103 | ||||
| chr15:45200496-45200584 | Common:1; Rare:28 | ||||
| chr15:48421658-48421983 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:48465643-48465813 | Rare:43; Clinvar (benign):1 | ||||
| chr15:60354152-60354364 | Rare:61 | ||||
| chr15:73927695-73927865 | Common:1; Rare:50 | ||||
| chr15:84631314-84631473 | Common:3; Rare:44 | ||||
| chr15:101276626-101276711 | Rare:36 | ||||
| chr16:3020903-3021287 | Rare:116 | ||||
| chr16:21820405-21820505 | Rare:26 | ||||
| chr16:30875331-30875465 | Rare:43 | ||||
| chr16:56617417-56617552 | Common:2; Rare:27 | ||||
| chr16:72664962-72665153 | Rare:60 | ||||
| chr16:74368127-74368367 | Common:1; Rare:69 | ||||
| chr17:909816-909897 | Common:2; Rare:17 |