| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46250191-46250448 | Common:3; Rare:79 | ||||
| chr22:46267804-46268027 | Common:1; Rare:60 | ||||
| chr22:46296580-46296930 | Common:2; Rare:107 | ||||
| chr22:46335580-46335769 | Common:3; Rare:80; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:46336724-46337124 | Common:1; Rare:105 | ||||
| chr22:46377946-46378346 | Common:4; Rare:161 | ||||
| chr22:46537588-46537723 | Common:2; Rare:64 | ||||
| chr22:46576945-46577105 | Common:1; Rare:68 | ||||
| chr22:46694140-46694540 | Common:13; Rare:116 | ||||
| chr22:46737680-46738060 | Common:1; Rare:87 | ||||
| chr22:46738182-46738472 | Common:7; Rare:77 | ||||
| chr22:46762453-46762679 | Common:3; Rare:85 | ||||
| chr22:49827821-49827952 | Common:1; Rare:49 | ||||
| chr22:49853485-49853975 | Common:2; Rare:169 | ||||
| chr22:49918373-49918726 | Common:2; Rare:137; Clinvar (benign):1 |