| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31489739-31490139 | Common:3; Rare:163 | ||||
| chr22:31496066-31496289 | Common:1; Rare:60 | ||||
| chr22:31496348-31496595 | Common:3; Rare:78 | ||||
| chr22:31497006-31497062 | Rare:19 | ||||
| chr22:31753745-31754107 | Common:1; Rare:129 | ||||
| chr22:32474607-32474740 | Common:2; Rare:41; Clinvar:1 | ||||
| chr22:32474968-32475333 | Common:2; Rare:122; Clinvar (benign):1 | ||||
| chr22:35257416-35257529 | Common:1; Rare:38 | ||||
| chr22:35299792-35299973 | Common:2; Rare:55 | ||||
| chr22:36239500-36239707 | Rare:65 | ||||
| chr22:36285656-36285960 | Rare:114; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:36387811-36388032 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36507015-36507168 | Common:3; Rare:53 | ||||
| chr22:36529074-36529322 | Common:1; Rare:80 | ||||
| chr22:37019402-37019778 | Common:5; Rare:108 |