| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:31472924-31473326 | Common:2; Rare:123 | ||||
| chr15:31473384-31473784 | Common:7; Rare:81 | ||||
| chr15:31483008-31483413 | Common:5; Rare:173 | ||||
| chr15:31488100-31488698 | Common:4; Rare:119 | ||||
| chr15:31708884-31709060 | Common:6; Rare:49 | ||||
| chr15:32634910-32635210 | Common:2; Rare:83 | ||||
| chr15:32637024-32637230 | Rare:74; Clinvar (pathogenic):1 | ||||
| chr15:32908293-32908860 | Common:9; Rare:394; Clinvar (benign):3 | ||||
| chr15:33898293-33898693 | Common:15; Rare:129 | ||||
| chr15:33915805-33916205 | Common:1; Rare:133 | ||||
| chr15:34237325-34237725 | Common:5; Rare:143; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr15:34327986-34328824 | Common:13; Rare:169 | ||||
| chr15:34328787-34329187 | Common:5; Rare:84 | ||||
| chr15:34331993-34332735 | Common:9; Rare:193 | ||||
| chr15:34333191-34333824 | Common:20; Rare:308 |