| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67429409-67429738 | Common:2; Rare:43 | ||||
| chr16:67429758-67429877 | Rare:26 | ||||
| chr16:67434344-67434421 | Rare:15 | ||||
| chr16:67435712-67436088 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:67436116-67436385 | Rare:96; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr16:67563372-67563422 | Rare:15 | ||||
| chr16:68297150-68297292 | Common:1; Rare:34 | ||||
| chr16:68365237-68365344 | Common:1; Rare:32 | ||||
| chr16:68366469-68366861 | Common:1; Rare:85 | ||||
| chr16:68381565-68381594 | Rare:6 | ||||
| chr16:68386601-68386865 | Rare:60 | ||||
| chr16:69323975-69324214 | Common:2; Rare:55 | ||||
| chr16:69979410-69979435 | Rare:3 | ||||
| chr16:69982368-69982542 | Common:2; Rare:63 | ||||
| chr16:70065063-70065213 | Rare:43 |