| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43493025-43493340 | Common:2; Rare:105 | ||||
| chr15:43510669-43511123 | Rare:177 | ||||
| chr15:43517347-43517653 | Common:2; Rare:61 | ||||
| chr15:43648812-43649036 | Common:3; Rare:94 | ||||
| chr15:43746221-43746704 | Common:3; Rare:189 | ||||
| chr15:43776915-43777119 | Common:1; Rare:64 | ||||
| chr15:43799131-43799235 | Common:2; Rare:31 | ||||
| chr15:43824495-43824882 | Common:2; Rare:115 | ||||
| chr15:43826905-43827044 | Rare:60 | ||||
| chr15:44194379-44194562 | Rare:38 | ||||
| chr15:44195262-44195439 | Common:2; Rare:53 | ||||
| chr15:44288367-44289354 | Common:41; Rare:395 | ||||
| chr15:44427075-44427868 | Common:5; Rare:209 | ||||
| chr15:44536663-44537401 | Common:3; Rare:242 | ||||
| chr15:44663551-44663722 | Rare:99; Clinvar:12; Clinvar (benign):6 |