| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39020816-39021182 | Common:2; Rare:87 | ||||
| chr22:39040526-39040891 | Common:3; Rare:67 | ||||
| chr22:39076972-39077294 | Common:1; Rare:71 | ||||
| chr22:39319578-39319918 | Common:4; Rare:126 | ||||
| chr22:39320305-39320432 | Common:3; Rare:33 | ||||
| chr22:39349801-39350017 | Common:1; Rare:67 | ||||
| chr22:39399646-39399805 | Common:3; Rare:65 | ||||
| chr22:39502193-39502405 | Rare:62 | ||||
| chr22:39532661-39533055 | Common:2; Rare:151 | ||||
| chr22:40044121-40044346 | Common:2; Rare:50 | ||||
| chr22:40044518-40044862 | Common:2; Rare:81 | ||||
| chr22:40177753-40177982 | Rare:72 | ||||
| chr22:40346389-40346585 | Common:1; Rare:92; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40346690-40346810 | Rare:45; Clinvar (benign):2 | ||||
| chr22:40370553-40370672 | Rare:50 |