| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319593-39319768 | Common:3; Rare:81 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40636668-40637012 | Common:2; Rare:96 | ||||
| chr22:40856939-40857120 | Common:1; Rare:67; Clinvar:1 | ||||
| chr22:41621032-41621368 | Common:7; Rare:127 | ||||
| chr22:42070761-42070971 | Common:2; Rare:46 | ||||
| chr22:42079632-42079763 | Common:1; Rare:39 | ||||
| chr22:42090740-42090945 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42649329-42649482 | Common:1; Rare:60 | ||||
| chr22:42857184-42857474 | Common:3; Rare:120 | ||||
| chr22:45163804-45164003 | Common:2; Rare:72 | ||||
| chr22:46053675-46053863 | Rare:64 | ||||
| chr22:46250282-46250364 | Common:1; Rare:24 | ||||
| chr22:46296632-46296922 | Common:2; Rare:99 |