| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43510638-43510977 | Rare:115 | ||||
| chr15:43648830-43649021 | Common:2; Rare:80 | ||||
| chr15:43746279-43746446 | Common:1; Rare:63 | ||||
| chr15:43769980-43770306 | Common:1; Rare:56 | ||||
| chr15:43777114-43777386 | Rare:64 | ||||
| chr15:44536663-44537200 | Common:1; Rare:162 | ||||
| chr15:44711314-44711622 | Rare:91; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711969 | Rare:23 | ||||
| chr15:45201094-45201151 | Common:1; Rare:27 | ||||
| chr15:45378537-45378743 | Common:3; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:45587177-45587277 | Rare:21 | ||||
| chr15:45587286-45587474 | Common:1; Rare:57; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:47718041-47718282 | Common:1; Rare:57 | ||||
| chr15:48178128-48178241 | Common:1; Rare:46 | ||||
| chr15:48331367-48331465 | Rare:32 |