| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43510602-43511102 | Rare:184 | ||||
| chr15:43746285-43746424 | Common:1; Rare:49 | ||||
| chr15:44536361-44536653 | Common:1; Rare:60 | ||||
| chr15:44536666-44537206 | Common:1; Rare:166 | ||||
| chr15:44711341-44711611 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45023033-45023241 | Common:3; Rare:52 | ||||
| chr15:45114141-45114327 | Common:2; Rare:39 | ||||
| chr15:45378482-45378658 | Common:3; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr15:45587104-45587226 | Rare:18 | ||||
| chr15:45587312-45587446 | Rare:43; Clinvar:4 | ||||
| chr15:47183979-47184390 | Common:2; Rare:132 | ||||
| chr15:48178128-48178446 | Common:1; Rare:98 | ||||
| chr15:48331367-48331465 | Rare:32 | ||||
| chr15:48878017-48878167 | Rare:53 | ||||
| chr15:49046355-49046617 | Common:2; Rare:93 |