| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68277645-68277804 | Common:2; Rare:47 | ||||
| chr15:68817570-68817709 | Common:1; Rare:51 | ||||
| chr15:68820758-68820810 | Rare:20 | ||||
| chr15:68820834-68821090 | Rare:73 | ||||
| chr15:68930351-68930583 | Common:3; Rare:73 | ||||
| chr15:69160342-69160668 | Common:4; Rare:98 | ||||
| chr15:69298793-69298955 | Common:3; Rare:36 | ||||
| chr15:69452691-69453020 | Common:5; Rare:137 | ||||
| chr15:70892371-70892711 | Common:1; Rare:73 | ||||
| chr15:71096809-71096914 | Rare:17 | ||||
| chr15:71547221-71547269 | Rare:10 | ||||
| chr15:71547274-71547352 | Rare:23 | ||||
| chr15:72118010-72118434 | Common:3; Rare:149 | ||||
| chr15:72231137-72231479 | Common:3; Rare:108 | ||||
| chr15:72375611-72375761 | Rare:34; Clinvar (pathogenic):3 |