| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42495462-42495708 | Common:2; Rare:69 | ||||
| chr15:42515033-42515307 | Common:1; Rare:54 | ||||
| chr15:42548702-42548881 | Common:2; Rare:95 | ||||
| chr15:43330543-43330727 | Common:1; Rare:66 | ||||
| chr15:43371030-43371189 | Common:1; Rare:35 | ||||
| chr15:43510638-43511086 | Rare:167 | ||||
| chr15:43648959-43649024 | Rare:26 | ||||
| chr15:43746285-43746689 | Common:1; Rare:166 | ||||
| chr15:43776961-43777079 | Rare:33 | ||||
| chr15:43777114-43777412 | Rare:65 | ||||
| chr15:43826870-43827028 | Rare:59 | ||||
| chr15:44288394-44288780 | Common:39; Rare:227 | ||||
| chr15:44536663-44537401 | Common:3; Rare:242 | ||||
| chr15:44711360-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711856-44711983 | Rare:25 |