| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43746257-43746704 | Common:3; Rare:175 | ||||
| chr15:43776955-43777112 | Common:1; Rare:46 | ||||
| chr15:43777114-43777409 | Rare:65 | ||||
| chr15:43792863-43793094 | Common:1; Rare:68 | ||||
| chr15:43824516-43824805 | Common:2; Rare:90 | ||||
| chr15:44288386-44288810 | Common:39; Rare:238 | ||||
| chr15:44427042-44427392 | Common:1; Rare:103 | ||||
| chr15:44536361-44536635 | Common:1; Rare:57 | ||||
| chr15:44536653-44537412 | Common:3; Rare:247 | ||||
| chr15:44663522-44663866 | Rare:160; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:44711297-44711616 | Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44712020 | Rare:32 | ||||
| chr15:44712630-44712815 | Rare:46 | ||||
| chr15:44728770-44729238 | Common:1; Rare:94 | ||||
| chr15:45023052-45023347 | Common:3; Rare:92 |