| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40350773-40351065 | Common:2; Rare:59 | ||||
| chr15:40358047-40358322 | Common:8; Rare:116 | ||||
| chr15:40358729-40358817 | Rare:17 | ||||
| chr15:40382700-40383031 | Common:2; Rare:134 | ||||
| chr15:40383355-40383387 | Rare:9 | ||||
| chr15:40405559-40405846 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40440752-40441013 | Rare:72 | ||||
| chr15:40441149-40441245 | Rare:26 | ||||
| chr15:40441253-40441342 | Common:1; Rare:21 | ||||
| chr15:40441652-40441778 | Rare:45 | ||||
| chr15:40470434-40470686 | Common:4; Rare:50 | ||||
| chr15:40470778-40471075 | Rare:90 | ||||
| chr15:40471199-40471357 | Rare:53; Clinvar:3 | ||||
| chr15:40564912-40565303 | Common:3; Rare:77 | ||||
| chr15:40569176-40569387 | Common:3; Rare:59 |