| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:26557206-26557511 | Common:3; Rare:62 | ||||
| chr22:26672650-26672786 | Common:2; Rare:34 | ||||
| chr22:27113284-27113537 | Common:2; Rare:51 | ||||
| chr22:27933354-27933436 | Rare:18 | ||||
| chr22:28799600-28799625 | Rare:3 | ||||
| chr22:28801496-28801645 | Common:1; Rare:22 | ||||
| chr22:28802240-28802449 | Common:2; Rare:40 | ||||
| chr22:29031351-29031472 | Common:2; Rare:25 | ||||
| chr22:29032641-29032691 | Rare:8 | ||||
| chr22:29570180-29570469 | Common:1; Rare:52 | ||||
| chr22:30019351-30019505 | Common:1; Rare:47 | ||||
| chr22:30407271-30407565 | Common:1; Rare:70 | ||||
| chr22:30922233-30922350 | Rare:49 | ||||
| chr22:31345035-31345230 | Common:1; Rare:51 | ||||
| chr22:36288725-36289293 | Common:2; Rare:172; Clinvar:5; Clinvar (benign):10 |