| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24555821-24556071 | Rare:77 | ||||
| chr22:26483772-26483883 | Common:4; Rare:47; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:26590071-26590220 | Common:3; Rare:63 | ||||
| chr22:27919170-27919527 | Common:5; Rare:155 | ||||
| chr22:28741798-28742082 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28800322-28800737 | Common:5; Rare:150 | ||||
| chr22:29267835-29268348 | Common:2; Rare:150 | ||||
| chr22:29603271-29603581 | Common:3; Rare:71 | ||||
| chr22:29767053-29767495 | Common:4; Rare:152 | ||||
| chr22:30289483-30289861 | Common:3; Rare:95 | ||||
| chr22:30356729-30357007 | Common:1; Rare:96 | ||||
| chr22:30607105-30607315 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:31080983-31081454 | Common:3; Rare:121 | ||||
| chr22:31082703-31082945 | Rare:44 |