| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:27897556-27897818 | Rare:49 | ||||
| chr22:27919177-27919557 | Common:5; Rare:163 | ||||
| chr22:28741776-28742068 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):7 | ||||
| chr22:28742541-28742705 | Common:1; Rare:38 | ||||
| chr22:28800430-28800702 | Common:5; Rare:103 | ||||
| chr22:29268196-29268346 | Rare:58 | ||||
| chr22:29388431-29388720 | Rare:95 | ||||
| chr22:29767063-29767405 | Common:4; Rare:107 | ||||
| chr22:29767499-29767561 | Common:1; Rare:31 | ||||
| chr22:30266225-30266426 | Rare:38 | ||||
| chr22:30266848-30266934 | Rare:11 | ||||
| chr22:30326871-30327173 | Common:2; Rare:105 | ||||
| chr22:30356868-30357077 | Common:2; Rare:60 | ||||
| chr22:31107539-31107744 | Common:2; Rare:57 | ||||
| chr22:31160088-31160227 | Common:1; Rare:51 |