| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46634890-46635359 | Common:19; Rare:401 | ||||
| chr21:46635333-46635805 | Common:43; Rare:685 | ||||
| chr21:46635823-46636239 | Common:10; Rare:453 | ||||
| chr22:11065668-11066518 | |||||
| chr22:17084410-17085120 | Common:25; Rare:659; Clinvar:17; Clinvar (benign):11 | ||||
| chr22:17158830-17159514 | Common:38; Rare:782 | ||||
| chr22:17368652-17369052 | Common:1; Rare:107 | ||||
| chr22:17369031-17369139 | Common:1; Rare:29 | ||||
| chr22:17369065-17369809 | Common:7; Rare:663 | ||||
| chr22:17476865-17477667 | Common:13; Rare:321 | ||||
| chr22:17562860-17563430 | Common:6; Rare:119 | ||||
| chr22:17628624-17629024 | Common:11; Rare:702 | ||||
| chr22:17629229-17629629 | Common:3; Rare:83 | ||||
| chr22:17637688-17638108 | Common:4; Rare:144 | ||||
| chr22:17638192-17638988 | Common:9; Rare:726 |