| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46286109-46286697 | Common:14; Rare:369 | ||||
| chr21:46323682-46324235 | Common:5; Rare:359; Clinvar:6; Clinvar (benign):3 | ||||
| chr21:46324424-46325012 | Common:16; Rare:322 | ||||
| chr21:46458442-46459172 | Common:12; Rare:412 | ||||
| chr21:46634970-46635280 | Common:3; Rare:94 | ||||
| chr21:46635418-46635740 | Common:14; Rare:215 | ||||
| chr22:17084789-17085060 | Common:7; Rare:159; Clinvar:6; Clinvar (benign):3 | ||||
| chr22:17159172-17159385 | Common:11; Rare:175 | ||||
| chr22:17628693-17628926 | Common:2; Rare:146 | ||||
| chr22:17638644-17638830 | Rare:129 | ||||
| chr22:17706668-17706802 | Common:1; Rare:35 | ||||
| chr22:17774438-17774577 | Rare:54 | ||||
| chr22:18077797-18078050 | Common:10; Rare:148; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:18078390-18078830 | Common:3; Rare:257; Clinvar:26; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr22:18149500-18150171 | Common:4; Rare:185 |