| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241881242-241881373 | Rare:28 | ||||
| chr20:3785117-3785272 | Common:2; Rare:73 | ||||
| chr20:5115333-5115550 | Rare:46; Clinvar (pathogenic):1 | ||||
| chr20:50166077-50166334 | Rare:63 | ||||
| chr20:50191407-50191667 | Common:1; Rare:75 | ||||
| chr20:50292603-50292709 | Common:1; Rare:23 | ||||
| chr21:26967017-26967293 | Rare:68 | ||||
| chr21:46003140-46003668 | Common:7; Rare:199; Clinvar:26; Clinvar (benign):22 | ||||
| chr21:46124652-46124888 | Common:5; Rare:105; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20702640-20702860 | Common:2; Rare:47 | ||||
| chr22:46052861-46052972 | Common:1; Rare:21 | ||||
| chr22:50526968-50527185 | Rare:71; Clinvar (pathogenic):1 | ||||
| chr3:12663465-12663599 | Common:2; Rare:41 | ||||
| chr3:37244192-37244287 | Common:2; Rare:26 | ||||
| chr3:40453142-40453417 | Common:6; Rare:66 |