| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17774392-17774585 | Rare:67 | ||||
| chr22:18077788-18078032 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149696-18150005 | Common:1; Rare:58 | ||||
| chr22:18150052-18150179 | Common:1; Rare:35 | ||||
| chr22:19178401-19178537 | Common:1; Rare:41 | ||||
| chr22:19291690-19291887 | Common:9; Rare:63 | ||||
| chr22:19432284-19432616 | Common:4; Rare:140 | ||||
| chr22:19447680-19447876 | Common:2; Rare:80 | ||||
| chr22:19479090-19479471 | Common:4; Rare:139 | ||||
| chr22:19479685-19479971 | Common:4; Rare:80 | ||||
| chr22:19854787-19855033 | Rare:93 | ||||
| chr22:19881105-19881487 | Common:3; Rare:98 | ||||
| chr22:19941720-19941886 | Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020873-20021141 | Common:1; Rare:87 | ||||
| chr22:20079916-20080302 | Common:1; Rare:125 |