| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70289395-70289746 | Rare:131; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:70346772-70346951 | Common:1; Rare:87 | ||||
| chr16:70454277-70454638 | Common:2; Rare:96 | ||||
| chr16:70523424-70523896 | Common:3; Rare:171; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70679374-70679649 | Rare:63 | ||||
| chr16:71808742-71808876 | Common:1; Rare:70 | ||||
| chr16:71808971-71809338 | Common:3; Rare:121 | ||||
| chr16:71845905-71846025 | Common:1; Rare:37 | ||||
| chr16:71884603-71884848 | Common:1; Rare:32 | ||||
| chr16:71895250-71895572 | Common:2; Rare:124 | ||||
| chr16:72008447-72008814 | Common:6; Rare:148; Clinvar (benign):2 | ||||
| chr16:72093538-72093972 | Common:1; Rare:109 | ||||
| chr16:73059005-73059159 | Rare:23 | ||||
| chr16:74296759-74296983 | Rare:87 | ||||
| chr16:74666859-74667107 | Common:1; Rare:76 |