| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21982748-21982897 | Rare:37 | ||||
| chr22:23786833-23787075 | Common:3; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:23857617-23857916 | Common:2; Rare:105 | ||||
| chr22:23894242-23894499 | Common:3; Rare:89 | ||||
| chr22:24011013-24011323 | Common:43; Rare:168 | ||||
| chr22:24270636-24270940 | Common:3; Rare:114 | ||||
| chr22:24555878-24556060 | Rare:53 | ||||
| chr22:26483784-26484049 | Common:9; Rare:124; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:26512428-26512559 | Common:1; Rare:58 | ||||
| chr22:27797017-27797089 | Rare:18 | ||||
| chr22:27801049-27801296 | Common:2; Rare:55 | ||||
| chr22:27801713-27801857 | Common:1; Rare:31 | ||||
| chr22:27919195-27919510 | Common:5; Rare:139 | ||||
| chr22:28741800-28742052 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28800379-28800702 | Common:5; Rare:114 |