| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46002046-46002321 | Common:1; Rare:97; Clinvar:9; Clinvar (benign):10 | ||||
| chr21:46184404-46184697 | Common:3; Rare:27 | ||||
| chr21:46286252-46286407 | Common:4; Rare:57 | ||||
| chr21:46323830-46324199 | Common:2; Rare:127; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46635472-46635747 | Common:5; Rare:90 | ||||
| chr22:17159193-17159342 | Common:5; Rare:70 | ||||
| chr22:17628694-17628872 | Common:1; Rare:62 | ||||
| chr22:17638696-17638827 | Rare:48 | ||||
| chr22:18077819-18078022 | Common:4; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19178437-19178527 | Common:1; Rare:26 | ||||
| chr22:19432303-19432599 | Common:4; Rare:127 | ||||
| chr22:19447677-19447774 | Common:1; Rare:48 | ||||
| chr22:19478953-19479071 | Rare:40 | ||||
| chr22:19479107-19479457 | Common:4; Rare:130 | ||||
| chr22:19479675-19479956 | Common:4; Rare:74 |