| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72686154-72686220 | Common:2; Rare:25; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633259-73633595 | Common:2; Rare:126 | ||||
| chr15:73926288-73926476 | Rare:50 | ||||
| chr15:73994578-73994797 | Common:1; Rare:47 | ||||
| chr15:74202776-74203049 | Common:1; Rare:70; Clinvar:2 | ||||
| chr15:74461101-74461307 | Rare:64 | ||||
| chr15:74540904-74541271 | Common:4; Rare:128 | ||||
| chr15:74615632-74615898 | Common:3; Rare:87 | ||||
| chr15:74695969-74696188 | Rare:61 | ||||
| chr15:74873275-74873494 | Common:6; Rare:66 | ||||
| chr15:74890005-74890076 | Rare:36; Clinvar (pathogenic):1 | ||||
| chr15:75335967-75336092 | Common:1; Rare:56 | ||||
| chr15:75347501-75347865 | Common:2; Rare:91 | ||||
| chr15:75368585-75368738 | Rare:43 | ||||
| chr15:75455795-75455967 | Rare:56 |