| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20858805-20859093 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20982196-20982363 | Common:2; Rare:40; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21002061-21002250 | Common:4; Rare:71 | ||||
| chr22:21642055-21642381 | Common:2; Rare:102 | ||||
| chr22:21665780-21666079 | Common:1; Rare:82 | ||||
| chr22:21694621-21694800 | Rare:60 | ||||
| chr22:23857793-23857916 | Common:2; Rare:38 | ||||
| chr22:23894205-23894544 | Common:3; Rare:124 | ||||
| chr22:23894577-23894890 | Common:3; Rare:125; Clinvar:1 | ||||
| chr22:24245064-24245182 | Rare:21 | ||||
| chr22:24270684-24270962 | Common:3; Rare:100 | ||||
| chr22:24555863-24556044 | Rare:57 | ||||
| chr22:25742054-25742266 | Common:1; Rare:44 | ||||
| chr22:26483757-26484140 | Common:9; Rare:170; Clinvar:5; Clinvar (benign):2 | ||||
| chr22:26512410-26512550 | Common:1; Rare:60 |