| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41230970-41231382 | Rare:319 | ||||
| chr15:41402368-41402640 | Common:10; Rare:200; Clinvar:4; Clinvar (benign):2 | ||||
| chr15:41416734-41417236 | Common:10; Rare:385 | ||||
| chr15:41492980-41493500 | Common:1; Rare:120 | ||||
| chr15:41493707-41493914 | Rare:166 | ||||
| chr15:41544179-41544387 | Common:1; Rare:178 | ||||
| chr15:41558677-41559022 | Common:1; Rare:102 | ||||
| chr15:41558980-41559290 | Common:2; Rare:136 | ||||
| chr15:41621123-41621292 | Common:1; Rare:43 | ||||
| chr15:41660243-41660554 | Rare:215 | ||||
| chr15:41660682-41660845 | Rare:83 | ||||
| chr15:41774063-41774592 | Common:3; Rare:294 | ||||
| chr15:41827881-41828171 | Common:4; Rare:108 | ||||
| chr15:41972456-41972919 | Common:4; Rare:243 | ||||
| chr15:42155900-42156340 | Common:4; Rare:148 |