| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92882387-92882732 | Common:3; Rare:106 | ||||
| chr15:94234495-94234603 | Rare:15 | ||||
| chr15:94287859-94288020 | Rare:30 | ||||
| chr15:94400547-94400840 | Common:1; Rare:60 | ||||
| chr15:95326862-95327034 | Common:1; Rare:56 | ||||
| chr15:95327283-95327574 | Common:1; Rare:81 | ||||
| chr15:95329469-95329549 | Rare:14 | ||||
| chr15:96321783-96321968 | Rare:36 | ||||
| chr15:96327102-96327415 | Common:5; Rare:58 | ||||
| chr15:96331706-96331731 | Rare:6 | ||||
| chr15:96333977-96334157 | Rare:61 | ||||
| chr15:96337149-96337451 | Common:5; Rare:89; Clinvar (pathogenic):1 | ||||
| chr15:96354042-96354409 | Common:4; Rare:80 | ||||
| chr15:98547359-98547480 | Common:1; Rare:22 | ||||
| chr15:98630732-98630875 | Rare:20 |