| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:26512428-26512552 | Common:1; Rare:55 | ||||
| chr22:26590077-26590220 | Common:3; Rare:58 | ||||
| chr22:27919177-27919510 | Common:5; Rare:145 | ||||
| chr22:28741789-28742078 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:28742413-28742702 | Common:1; Rare:68 | ||||
| chr22:28800054-28800356 | Common:2; Rare:85 | ||||
| chr22:28800528-28800709 | Common:4; Rare:74 | ||||
| chr22:29205806-29206058 | Common:1; Rare:65 | ||||
| chr22:29267894-29268348 | Common:2; Rare:130 | ||||
| chr22:29480068-29480427 | Common:2; Rare:116 | ||||
| chr22:29480683-29480985 | Common:1; Rare:116; Clinvar (pathogenic):1 | ||||
| chr22:29603383-29603663 | Rare:67; Clinvar:1 | ||||
| chr22:29766924-29767015 | Common:1; Rare:27 | ||||
| chr22:29767053-29767510 | Common:4; Rare:157 | ||||
| chr22:30080202-30080504 | Common:2; Rare:80 |