| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:60397948-60398134 | Common:2; Rare:36 | ||||
| chr15:60478921-60479247 | Common:4; Rare:141 | ||||
| chr15:60592473-60592751 | Common:1; Rare:74 | ||||
| chr15:61229216-61229549 | Common:1; Rare:75 | ||||
| chr15:62060364-62060513 | Rare:59 | ||||
| chr15:62390430-62390643 | Common:1; Rare:106 | ||||
| chr15:63042451-63042943 | Common:6; Rare:151; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63043244-63043587 | Rare:79 | ||||
| chr15:63048335-63048689 | Common:4; Rare:134; Clinvar:5; Clinvar (benign):4 | ||||
| chr15:63121709-63121866 | Rare:47 | ||||
| chr15:63157133-63157212 | Rare:15 | ||||
| chr15:63157401-63157550 | Common:2; Rare:65 | ||||
| chr15:63157761-63157976 | Rare:42 | ||||
| chr15:63158019-63158189 | Common:3; Rare:41 | ||||
| chr15:63189393-63189646 | Common:2; Rare:88 |