| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20858729-20859093 | Common:5; Rare:186; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20917251-20917516 | Rare:96 | ||||
| chr22:20979345-20979670 | Common:6; Rare:124 | ||||
| chr22:20982196-20982361 | Common:2; Rare:39; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002002-21002223 | Common:4; Rare:90 | ||||
| chr22:21629954-21630154 | Common:2; Rare:82 | ||||
| chr22:21642015-21642402 | Common:2; Rare:120 | ||||
| chr22:21651922-21652192 | Common:2; Rare:57 | ||||
| chr22:21867606-21867915 | Common:2; Rare:99 | ||||
| chr22:22508703-22508913 | Rare:69 | ||||
| chr22:22520266-22520455 | Common:4; Rare:40 | ||||
| chr22:23180476-23180538 | Common:2; Rare:26 | ||||
| chr22:23750954-23751201 | Common:2; Rare:84 | ||||
| chr22:23765973-23766174 | Common:1; Rare:90; Clinvar (benign):2 | ||||
| chr22:23767862-23768040 | Rare:57 |