| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21599290-21600160 | Common:24; Rare:1060 | ||||
| chr16:21600191-21600591 | Rare:86 | ||||
| chr16:21611660-21612180 | Common:8; Rare:214 | ||||
| chr16:21704683-21705083 | Common:4; Rare:145; Clinvar (benign):1 | ||||
| chr16:21952371-21952771 | Rare:89 | ||||
| chr16:21952860-21953446 | Common:7; Rare:814; Clinvar (benign):21 | ||||
| chr16:21953669-21954069 | Rare:71 | ||||
| chr16:22007390-22007840 | Common:6; Rare:147 | ||||
| chr16:22007820-22008200 | Rare:238 | ||||
| chr16:22008220-22008800 | Common:4; Rare:198 | ||||
| chr16:22205933-22206432 | Common:6; Rare:626 | ||||
| chr16:22206492-22206892 | Common:2; Rare:92 | ||||
| chr16:22286408-22286808 | Common:2; Rare:76 | ||||
| chr16:22286798-22286964 | Rare:65 | ||||
| chr16:22296454-22297483 | Common:29; Rare:1105 |