| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20982196-20982363 | Common:2; Rare:40; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21002092-21002211 | Common:3; Rare:45 | ||||
| chr22:21642025-21642346 | Common:2; Rare:98 | ||||
| chr22:23786852-23787025 | Common:1; Rare:62; Clinvar:3 | ||||
| chr22:23857800-23857920 | Common:2; Rare:39 | ||||
| chr22:23894054-23894534 | Common:5; Rare:144 | ||||
| chr22:23894578-23894912 | Common:3; Rare:134; Clinvar:1 | ||||
| chr22:24271080-24271190 | Common:1; Rare:53 | ||||
| chr22:24554957-24555444 | Common:4; Rare:181 | ||||
| chr22:24555884-24556066 | Rare:53 | ||||
| chr22:26483771-26483964 | Common:4; Rare:80; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512552 | Common:1; Rare:55 | ||||
| chr22:26590085-26590220 | Common:3; Rare:54 | ||||
| chr22:27919171-27919527 | Common:5; Rare:155 | ||||
| chr22:28741806-28742078 | Common:2; Rare:79 |