| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46002046-46002388 | Common:1; Rare:115; Clinvar:13; Clinvar (benign):12 | ||||
| chr21:46097552-46097635 | Common:3; Rare:18 | ||||
| chr21:46184409-46184697 | Common:3; Rare:27 | ||||
| chr21:46286217-46286403 | Common:4; Rare:72 | ||||
| chr21:46323863-46324177 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458684-46459070 | Common:3; Rare:132 | ||||
| chr22:17158942-17159375 | Common:11; Rare:169 | ||||
| chr22:17628602-17628860 | Common:2; Rare:80 | ||||
| chr22:17638672-17638859 | Rare:66 | ||||
| chr22:17706716-17706822 | Rare:34 | ||||
| chr22:18077861-18078028 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18110650-18110807 | Rare:40 | ||||
| chr22:18149825-18149991 | Common:1; Rare:30 | ||||
| chr22:19178449-19178516 | Common:1; Rare:16 | ||||
| chr22:19291707-19291917 | Common:9; Rare:64 |