| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28679737-28679989 | Common:3; Rare:87 | ||||
| chr22:28741126-28741428 | Common:7; Rare:49 | ||||
| chr22:28741573-28741640 | Rare:13; Clinvar (benign):1 | ||||
| chr22:28741773-28742143 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):7 | ||||
| chr22:28742250-28742711 | Common:1; Rare:126 | ||||
| chr22:28772570-28772833 | Common:6; Rare:82 | ||||
| chr22:28773043-28773146 | Common:4; Rare:38 | ||||
| chr22:28773275-28773734 | Common:5; Rare:122 | ||||
| chr22:28799899-28800012 | Rare:41 | ||||
| chr22:28800041-28800219 | Common:1; Rare:56 | ||||
| chr22:28800450-28800779 | Common:6; Rare:126 | ||||
| chr22:28800879-28801016 | Rare:20 | ||||
| chr22:29266953-29267300 | Common:1; Rare:83 | ||||
| chr22:29267696-29268381 | Common:3; Rare:206 | ||||
| chr22:29268657-29268747 | Rare:42 |