| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69160342-69160635 | Common:3; Rare:87 | ||||
| chr15:69298756-69298961 | Common:3; Rare:43 | ||||
| chr15:69314301-69314383 | Common:1; Rare:13 | ||||
| chr15:69414216-69414453 | Rare:85 | ||||
| chr15:72118168-72118417 | Common:2; Rare:77 | ||||
| chr15:72231160-72231504 | Common:3; Rare:107 | ||||
| chr15:72375958-72376070 | Common:2; Rare:50; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686097-72686220 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73994600-73994716 | Rare:17 | ||||
| chr15:74461125-74461293 | Rare:55 | ||||
| chr15:74889958-74890064 | Rare:42 | ||||
| chr15:75201828-75201886 | Rare:20 | ||||
| chr15:75625627-75625899 | Common:1; Rare:61 | ||||
| chr15:75903848-75903956 | Rare:47 | ||||
| chr15:76311393-76311629 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):5 |