| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43510602-43510964 | Rare:112 | ||||
| chr15:43592948-43593108 | Rare:8 | ||||
| chr15:43648709-43649022 | Common:3; Rare:133 | ||||
| chr15:43746285-43746704 | Common:2; Rare:169 | ||||
| chr15:43776926-43777112 | Common:1; Rare:60 | ||||
| chr15:43777114-43777439 | Rare:69 | ||||
| chr15:43792674-43793129 | Common:1; Rare:130 | ||||
| chr15:44288396-44288749 | Common:38; Rare:219 | ||||
| chr15:44536663-44537425 | Common:3; Rare:246 | ||||
| chr15:44711351-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711977 | Rare:24 | ||||
| chr15:45023068-45023256 | Common:3; Rare:52 | ||||
| chr15:45114106-45114345 | Common:2; Rare:50 | ||||
| chr15:45129815-45130086 | Rare:57 | ||||
| chr15:45153336-45153427 | Rare:26 |