| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46323830-46324224 | Common:3; Rare:145; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46324453-46324653 | Common:3; Rare:75 | ||||
| chr21:46458680-46459070 | Common:3; Rare:133 | ||||
| chr21:46635476-46635761 | Common:6; Rare:94 | ||||
| chr21:46636157-46636462 | Common:1; Rare:60 | ||||
| chr22:17084791-17085122 | Common:6; Rare:114; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:17159175-17159393 | Common:6; Rare:108 | ||||
| chr22:17569862-17569938 | Rare:13 | ||||
| chr22:17628648-17628866 | Common:2; Rare:75 | ||||
| chr22:17638677-17638817 | Rare:49 | ||||
| chr22:17774390-17774579 | Rare:65 | ||||
| chr22:18077791-18078032 | Common:5; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18150018-18150188 | Common:1; Rare:46 | ||||
| chr22:19178445-19178522 | Common:1; Rare:21 | ||||
| chr22:19291690-19291930 | Common:10; Rare:73 |