| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28741789-28742082 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:28800395-28800703 | Common:5; Rare:112 | ||||
| chr22:29267901-29268339 | Common:2; Rare:125 | ||||
| chr22:29581085-29581211 | Common:2; Rare:36 | ||||
| chr22:30326882-30327173 | Common:2; Rare:100 | ||||
| chr22:30356868-30357015 | Common:1; Rare:47 | ||||
| chr22:31081176-31081341 | Common:1; Rare:42 | ||||
| chr22:31107517-31107728 | Common:2; Rare:60 | ||||
| chr22:31212109-31212314 | Rare:68 | ||||
| chr22:31399467-31399648 | Rare:50 | ||||
| chr22:31496412-31496547 | Common:1; Rare:34 | ||||
| chr22:31630836-31631038 | Common:4; Rare:48 | ||||
| chr22:31662191-31662359 | Common:2; Rare:70 | ||||
| chr22:31750052-31750330 | Common:3; Rare:81 | ||||
| chr22:31753768-31754093 | Common:1; Rare:117 |