| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45404878-45405174 | Common:12; Rare:172 | ||||
| chr21:45455727-45455776 | Common:1; Rare:18 | ||||
| chr21:45981510-45981831 | Common:23; Rare:73; Clinvar (benign):2 | ||||
| chr21:46184399-46184736 | Common:4; Rare:33 | ||||
| chr21:46286233-46286640 | Common:6; Rare:137 | ||||
| chr21:46323841-46324170 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46324449-46324669 | Common:4; Rare:79 | ||||
| chr21:46458684-46459128 | Common:4; Rare:151 | ||||
| chr21:46635480-46635761 | Common:6; Rare:93 | ||||
| chr21:46636168-46636449 | Common:1; Rare:56 | ||||
| chr22:17158967-17159385 | Common:10; Rare:166 | ||||
| chr22:17628602-17628866 | Common:2; Rare:82 | ||||
| chr22:17638696-17638839 | Rare:51 | ||||
| chr22:17774410-17774581 | Rare:61 | ||||
| chr22:18077800-18078047 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):2 |