| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39399684-39399802 | Common:2; Rare:51 | ||||
| chr22:39502088-39502412 | Rare:96 | ||||
| chr22:39532667-39533037 | Common:2; Rare:143 | ||||
| chr22:40044121-40044362 | Common:2; Rare:56 | ||||
| chr22:40044527-40044875 | Common:2; Rare:82 | ||||
| chr22:40177793-40177999 | Rare:57 | ||||
| chr22:40346425-40346564 | Rare:59; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:40533767-40533971 | Rare:44 | ||||
| chr22:40636661-40637033 | Common:2; Rare:102 | ||||
| chr22:40819277-40819499 | Common:11; Rare:109 | ||||
| chr22:40856364-40857169 | Common:4; Rare:331; Clinvar:4 | ||||
| chr22:40951031-40951476 | Common:2; Rare:146 | ||||
| chr22:40951600-40951859 | Common:2; Rare:75 | ||||
| chr22:41091391-41091825 | Common:6; Rare:155 | ||||
| chr22:41286152-41286498 | Common:2; Rare:106 |