| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19432303-19432593 | Common:4; Rare:121 | ||||
| chr22:19447677-19447938 | Common:2; Rare:109 | ||||
| chr22:19479097-19479466 | Common:4; Rare:135 | ||||
| chr22:19525326-19525522 | Common:1; Rare:38 | ||||
| chr22:19854787-19854997 | Rare:73 | ||||
| chr22:19932449-19932706 | Rare:51 | ||||
| chr22:19941721-19941886 | Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020891-20021157 | Common:1; Rare:90 | ||||
| chr22:20079921-20080293 | Common:1; Rare:121 | ||||
| chr22:20116952-20117012 | Common:1; Rare:13 | ||||
| chr22:20117090-20117571 | Common:3; Rare:147 | ||||
| chr22:20319986-20320174 | Common:2; Rare:67 | ||||
| chr22:20394090-20394196 | Rare:28 | ||||
| chr22:20495781-20495986 | Common:2; Rare:78 | ||||
| chr22:20553006-20553171 | Common:1; Rare:40 |