| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46634193-46634901 | Common:6; Rare:235 | ||||
| chr21:46635049-46635239 | Common:2; Rare:51 | ||||
| chr21:46635382-46635761 | Common:15; Rare:240 | ||||
| chr21:46635887-46636025 | Common:4; Rare:62 | ||||
| chr22:11066020-11066269 | |||||
| chr22:17084695-17085081 | Common:11; Rare:318; Clinvar:9; Clinvar (benign):5 | ||||
| chr22:17158479-17158598 | Rare:25 | ||||
| chr22:17158867-17159412 | Common:28; Rare:502 | ||||
| chr22:17368620-17368970 | Common:3; Rare:116 | ||||
| chr22:17369093-17369518 | Common:2; Rare:160 | ||||
| chr22:17628592-17628961 | Common:5; Rare:296 | ||||
| chr22:17638469-17639002 | Common:2; Rare:292 | ||||
| chr22:17706566-17706966 | Common:3; Rare:128 | ||||
| chr22:17773512-17773631 | Rare:38 | ||||
| chr22:17773870-17774270 | Common:6; Rare:216 |