| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39076976-39077083 | Common:1; Rare:20 | ||||
| chr22:39319596-39319768 | Common:3; Rare:81 | ||||
| chr22:39349820-39350008 | Common:1; Rare:57 | ||||
| chr22:39399694-39399796 | Common:2; Rare:46 | ||||
| chr22:39502189-39502370 | Rare:48 | ||||
| chr22:39532688-39532904 | Common:2; Rare:91 | ||||
| chr22:40044119-40044327 | Common:2; Rare:44 | ||||
| chr22:40044518-40044880 | Common:2; Rare:85 | ||||
| chr22:40177793-40177954 | Rare:46 | ||||
| chr22:40346418-40346556 | Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40463414-40463475 | Rare:12 | ||||
| chr22:40636668-40637033 | Common:2; Rare:102 | ||||
| chr22:40819321-40819541 | Common:11; Rare:109 | ||||
| chr22:40856594-40856722 | Rare:52 | ||||
| chr22:40856934-40857154 | Common:1; Rare:90; Clinvar:3 |