| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43826937-43827039 | Rare:46 | ||||
| chr15:44288374-44288749 | Common:38; Rare:222 | ||||
| chr15:44458753-44459078 | Common:1; Rare:72 | ||||
| chr15:44536663-44536705 | Rare:6 | ||||
| chr15:44536843-44537458 | Common:3; Rare:220 | ||||
| chr15:44572771-44572864 | Rare:33; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:44711297-44711616 | Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711990 | Rare:26 | ||||
| chr15:44712636-44712966 | Common:1; Rare:75 | ||||
| chr15:44728716-44729211 | Common:1; Rare:98 | ||||
| chr15:45023052-45023248 | Common:3; Rare:53 | ||||
| chr15:45100467-45100539 | Rare:12 | ||||
| chr15:45100556-45100742 | Common:3; Rare:34 | ||||
| chr15:45102070-45102277 | Common:2; Rare:37 | ||||
| chr15:45113837-45113993 | Rare:36 |