| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39999448-39999848 | Common:4; Rare:111 | ||||
| chr22:40002193-40002593 | Common:2; Rare:85 | ||||
| chr22:40651736-40651913 | Common:6; Rare:105 | ||||
| chr22:41021954-41022108 | Rare:81 | ||||
| chr22:41022550-41022880 | Common:8; Rare:155 | ||||
| chr22:41092425-41092628 | Rare:185 | ||||
| chr22:41197425-41197670 | Common:3; Rare:114 | ||||
| chr22:41264680-41265030 | Common:2; Rare:166 | ||||
| chr22:41288290-41288640 | Common:2; Rare:112 | ||||
| chr22:41413510-41413790 | Common:4; Rare:113 | ||||
| chr22:41413901-41414077 | Rare:103 | ||||
| chr22:41448480-41448880 | Common:5; Rare:94 | ||||
| chr22:41666670-41666950 | Common:4; Rare:145 | ||||
| chr22:41667200-41667710 | Common:2; Rare:175 | ||||
| chr22:42067550-42067806 | Common:3; Rare:95; Clinvar (pathogenic):2 |