| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40044517-40044897 | Common:2; Rare:87 | ||||
| chr22:40177752-40177998 | Rare:73 | ||||
| chr22:40346434-40346588 | Rare:73; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr22:40636659-40637033 | Common:2; Rare:102 | ||||
| chr22:40856369-40857184 | Common:4; Rare:336; Clinvar:4 | ||||
| chr22:40951547-40951764 | Common:2; Rare:65 | ||||
| chr22:41091413-41091823 | Common:6; Rare:145 | ||||
| chr22:41286146-41286522 | Common:2; Rare:123 | ||||
| chr22:41367190-41367498 | Rare:88 | ||||
| chr22:41446431-41446546 | Rare:22 | ||||
| chr22:41446756-41446980 | Rare:96 | ||||
| chr22:41468610-41468813 | Common:2; Rare:54 | ||||
| chr22:41468997-41469175 | Rare:67 | ||||
| chr22:41515096-41515399 | Rare:56; Clinvar (benign):1 | ||||
| chr22:41515541-41515912 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):2 |