| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40953231-40953479 | Common:2; Rare:69 | ||||
| chr15:41116561-41116722 | Rare:53 | ||||
| chr15:41230592-41230992 | Common:1; Rare:165 | ||||
| chr15:41332504-41332932 | Common:2; Rare:177 | ||||
| chr15:41402446-41402572 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr15:41416930-41417204 | Common:4; Rare:120 | ||||
| chr15:41492860-41493530 | Common:1; Rare:140 | ||||
| chr15:41493755-41493874 | Rare:39 | ||||
| chr15:41544186-41544389 | Common:2; Rare:77 | ||||
| chr15:41558246-41559343 | Common:6; Rare:488 | ||||
| chr15:41620980-41621751 | Common:5; Rare:331 | ||||
| chr15:41621936-41622155 | Common:3; Rare:61 | ||||
| chr15:41660300-41660476 | Rare:52 | ||||
| chr15:41660676-41660776 | Rare:34 | ||||
| chr15:41774013-41774202 | Common:1; Rare:37 |