| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41333129-41333263 | Common:1; Rare:18 | ||||
| chr15:41333273-41333634 | Common:1; Rare:80 | ||||
| chr15:41402275-41402644 | Common:4; Rare:125; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:41416527-41416833 | Common:1; Rare:57 | ||||
| chr15:41416876-41417216 | Common:4; Rare:138 | ||||
| chr15:41477354-41477495 | Common:1; Rare:31 | ||||
| chr15:41493250-41493451 | Rare:46 | ||||
| chr15:41493554-41493907 | Rare:99 | ||||
| chr15:41494353-41494609 | Rare:56 | ||||
| chr15:41508226-41508309 | Rare:26 | ||||
| chr15:41544001-41544414 | Common:3; Rare:122 | ||||
| chr15:41558960-41559276 | Common:1; Rare:90 | ||||
| chr15:41559564-41559583 | Common:1; Rare:6 | ||||
| chr15:41621162-41621279 | Common:1; Rare:33 | ||||
| chr15:41621320-41621861 | Common:1; Rare:136 |