| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17369187-17369502 | Common:2; Rare:128 | ||||
| chr22:17369872-17369901 | Rare:5 | ||||
| chr22:17563151-17563491 | Common:5; Rare:67 | ||||
| chr22:17628650-17628853 | Common:2; Rare:72 | ||||
| chr22:17638550-17638907 | Common:1; Rare:106 | ||||
| chr22:17773718-17773783 | Common:1; Rare:16 | ||||
| chr22:17773879-17774126 | Common:1; Rare:61 | ||||
| chr22:18077807-18078058 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122364-19122706 | Common:4; Rare:90 | ||||
| chr22:19178366-19178521 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chr22:19178712-19178976 | Common:2; Rare:91; Clinvar (benign):1 | ||||
| chr22:19291654-19291969 | Common:12; Rare:111 | ||||
| chr22:19431685-19432080 | Rare:97 | ||||
| chr22:19432284-19432627 | Common:4; Rare:144 | ||||
| chr22:19447660-19447972 | Common:2; Rare:130 |