| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68365378-68365425 | Rare:5 | ||||
| chr15:69452701-69453020 | Common:5; Rare:132 | ||||
| chr15:70853957-70854251 | Rare:83 | ||||
| chr15:72118167-72118403 | Common:2; Rare:75 | ||||
| chr15:72231114-72231523 | Common:3; Rare:131 | ||||
| chr15:72375951-72376124 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72686129-72686220 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73926294-73926501 | Rare:56 | ||||
| chr15:73926872-73927147 | Common:1; Rare:72 | ||||
| chr15:73992176-73992406 | Rare:85 | ||||
| chr15:73994570-73994801 | Common:1; Rare:49 | ||||
| chr15:74173826-74173886 | Common:2; Rare:10 | ||||
| chr15:74461107-74461307 | Rare:62 | ||||
| chr15:74615576-74615884 | Common:4; Rare:99 | ||||
| chr15:74843113-74843237 | Common:1; Rare:36 |