| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22206614-22206773 | Common:1; Rare:33 | ||||
| chr16:22297125-22297508 | Common:4; Rare:200 | ||||
| chr16:22297797-22297955 | Common:1; Rare:38 | ||||
| chr16:22373969-22374082 | Common:1; Rare:35 | ||||
| chr16:22374341-22374744 | Common:1; Rare:137 | ||||
| chr16:22374789-22374946 | Rare:41 | ||||
| chr16:22436878-22437363 | Rare:159 | ||||
| chr16:22437415-22437625 | Common:2; Rare:62 | ||||
| chr16:22813973-22814202 | Common:1; Rare:45 | ||||
| chr16:23182620-23182780 | Common:1; Rare:35 | ||||
| chr16:23452660-23452831 | Rare:62; Clinvar (benign):1 | ||||
| chr16:23453021-23453296 | Rare:73 | ||||
| chr16:23510387-23510599 | Common:5; Rare:108 | ||||
| chr16:23510613-23510824 | Rare:44 | ||||
| chr16:23557094-23557600 | Common:4; Rare:184; Clinvar:1; Clinvar (benign):4 |