| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46458686-46459012 | Common:3; Rare:112 | ||||
| chr21:46635520-46635723 | Common:2; Rare:68 | ||||
| chr22:17159183-17159385 | Common:5; Rare:93 | ||||
| chr22:17628648-17628860 | Common:2; Rare:73 | ||||
| chr22:17638663-17638817 | Rare:53 | ||||
| chr22:18077814-18078022 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122389-19122650 | Common:3; Rare:60 | ||||
| chr22:19144642-19144818 | Common:2; Rare:63 | ||||
| chr22:19178462-19178537 | Common:1; Rare:19 | ||||
| chr22:19291696-19291917 | Common:10; Rare:69 | ||||
| chr22:19432303-19432606 | Common:4; Rare:129 | ||||
| chr22:19447667-19447721 | Rare:37 | ||||
| chr22:19479161-19479471 | Common:4; Rare:102 | ||||
| chr22:19854806-19855033 | Rare:88 | ||||
| chr22:19941722-19941878 | Rare:66; Clinvar:5; Clinvar (benign):4 |