| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67520958-67521260 | Common:5; Rare:119 | ||||
| chr15:67521632-67521713 | Rare:22 | ||||
| chr15:68054008-68054332 | Rare:83 | ||||
| chr15:68820729-68821074 | Rare:103 | ||||
| chr15:69414146-69414468 | Rare:108 | ||||
| chr15:69452688-69453014 | Common:5; Rare:136 | ||||
| chr15:70763467-70763814 | Common:2; Rare:123 | ||||
| chr15:70854061-70854293 | Rare:71 | ||||
| chr15:70892520-70892855 | Common:1; Rare:67 | ||||
| chr15:72118015-72118432 | Common:3; Rare:145 | ||||
| chr15:72231098-72231512 | Common:3; Rare:127 | ||||
| chr15:72375944-72376124 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474167-72474330 | Rare:60 | ||||
| chr15:72686116-72686220 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633298-73633595 | Common:2; Rare:112 |