| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319594-39319768 | Common:3; Rare:81 | ||||
| chr22:39349826-39350017 | Common:1; Rare:56 | ||||
| chr22:39399608-39399808 | Common:3; Rare:78 | ||||
| chr22:39502158-39502412 | Rare:75 | ||||
| chr22:39519575-39519672 | Rare:24 | ||||
| chr22:39520078-39520304 | Common:1; Rare:64 | ||||
| chr22:39521051-39521873 | Common:7; Rare:332 | ||||
| chr22:39532661-39532875 | Common:2; Rare:97 | ||||
| chr22:40044140-40044346 | Common:2; Rare:45 | ||||
| chr22:40044525-40044880 | Common:2; Rare:84 | ||||
| chr22:40045031-40045093 | Rare:16 | ||||
| chr22:40177793-40178046 | Rare:65 | ||||
| chr22:40346445-40346580 | Rare:61; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636656-40637012 | Common:2; Rare:98 | ||||
| chr22:40856369-40857179 | Common:4; Rare:334; Clinvar:4 |