| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20020880-20021171 | Common:1; Rare:96 | ||||
| chr22:20079916-20080299 | Common:1; Rare:125 | ||||
| chr22:20116959-20117655 | Common:5; Rare:207 | ||||
| chr22:20319992-20320160 | Common:2; Rare:56 | ||||
| chr22:20394060-20394194 | Rare:32 | ||||
| chr22:20495775-20495996 | Common:2; Rare:82 | ||||
| chr22:20507410-20507681 | Common:1; Rare:97 | ||||
| chr22:20523535-20523891 | Common:1; Rare:70 | ||||
| chr22:20917278-20917457 | Rare:72 | ||||
| chr22:20981974-20981990 | Rare:5 | ||||
| chr22:20982170-20982363 | Common:2; Rare:54; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21002002-21002251 | Common:5; Rare:99 | ||||
| chr22:21032554-21032650 | Rare:40 | ||||
| chr22:21642044-21642381 | Common:2; Rare:105 | ||||
| chr22:21651922-21652187 | Common:2; Rare:55 |