| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43812208-43812441 | Common:3; Rare:78 | ||||
| chr22:43955338-43955566 | Common:2; Rare:70 | ||||
| chr22:44024219-44024426 | Common:1; Rare:70 | ||||
| chr22:44668472-44668751 | Common:4; Rare:106 | ||||
| chr22:45163694-45164195 | Common:7; Rare:191 | ||||
| chr22:45671924-45672108 | Common:1; Rare:81 | ||||
| chr22:46053749-46053909 | Rare:59 | ||||
| chr22:46250260-46250404 | Common:2; Rare:43 | ||||
| chr22:46267841-46268037 | Common:1; Rare:61 | ||||
| chr22:46762517-46762693 | Common:3; Rare:62 | ||||
| chr22:48692709-48693015 | Common:6; Rare:83 | ||||
| chr22:49853571-49853899 | Common:2; Rare:121 | ||||
| chr22:50525547-50525685 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50582790-50583120 | Common:7; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628092-50628276 | Common:9; Rare:88; Clinvar:3; Clinvar (benign):1 |