| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856594-40856753 | Rare:64 | ||||
| chr22:41621018-41621370 | Common:7; Rare:131 | ||||
| chr22:41947114-41947204 | Rare:28 | ||||
| chr22:42070793-42070947 | Common:2; Rare:30 | ||||
| chr22:42090743-42090956 | Common:1; Rare:71 | ||||
| chr22:42614858-42615244 | Common:3; Rare:158 | ||||
| chr22:43955303-43955556 | Common:3; Rare:75 | ||||
| chr22:45163804-45164003 | Common:2; Rare:72 | ||||
| chr22:46250282-46250408 | Common:1; Rare:40 | ||||
| chr22:46296712-46296924 | Common:2; Rare:76 | ||||
| chr22:46335621-46335760 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:46762517-46762669 | Common:3; Rare:52 | ||||
| chr22:50783646-50783836 | Common:1; Rare:54 | ||||
| chr3:3126813-3126975 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chr3:9362984-9363098 | Common:1; Rare:44 |