| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38700919-38701006 | Rare:35 | ||||
| chr22:38982269-38982425 | Common:1; Rare:31 | ||||
| chr22:39319572-39319771 | Common:3; Rare:92 | ||||
| chr22:39532730-39533061 | Common:2; Rare:116 | ||||
| chr22:40044549-40044810 | Common:2; Rare:59 | ||||
| chr22:40346451-40346577 | Rare:57; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40370539-40370683 | Rare:58 | ||||
| chr22:40636621-40636974 | Common:2; Rare:109 | ||||
| chr22:40856430-40857158 | Common:2; Rare:297; Clinvar:3 | ||||
| chr22:40951055-40951470 | Common:2; Rare:135 | ||||
| chr22:40951598-40951862 | Common:2; Rare:77 | ||||
| chr22:41091706-41091831 | Common:1; Rare:52 | ||||
| chr22:41176505-41176751 | Common:2; Rare:77; Clinvar (benign):2 | ||||
| chr22:41285952-41286338 | Common:3; Rare:120 | ||||
| chr22:41446792-41447062 | Common:1; Rare:119 |