| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45987006-45987175 | Common:1; Rare:61; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:45987196-45987654 | Common:3; Rare:167; Clinvar:11; Clinvar (benign):7 | ||||
| chr21:46002236-46002640 | Common:2; Rare:134; Clinvar:21; Clinvar (benign):12 | ||||
| chr21:46097437-46097620 | Common:3; Rare:39 | ||||
| chr21:46113808-46114073 | Common:1; Rare:63; Clinvar:5; Clinvar (benign):1 | ||||
| chr21:46184390-46184756 | Common:5; Rare:34 | ||||
| chr21:46286250-46286396 | Common:4; Rare:54 | ||||
| chr21:46323789-46324211 | Common:2; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:17628706-17628866 | Common:1; Rare:51 | ||||
| chr22:17638696-17638817 | Rare:43 | ||||
| chr22:17774415-17774587 | Rare:63 | ||||
| chr22:18077758-18078018 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19432303-19432606 | Common:4; Rare:129 | ||||
| chr22:19479687-19479949 | Common:4; Rare:66 | ||||
| chr22:19854803-19854968 | Rare:57 |