| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68245192-68245410 | Common:1; Rare:70 | ||||
| chr16:68310922-68311062 | Common:1; Rare:67 | ||||
| chr16:69132488-69132656 | Rare:59 | ||||
| chr16:69187041-69187156 | Rare:42 | ||||
| chr16:69339551-69339821 | Common:1; Rare:109; Clinvar (benign):1 | ||||
| chr16:70114127-70114376 | Common:3; Rare:89 | ||||
| chr16:70289440-70289842 | Common:3; Rare:153; Clinvar:1 | ||||
| chr16:70346592-70346955 | Common:1; Rare:141 | ||||
| chr16:70523517-70523844 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71895294-71895578 | Common:3; Rare:104 | ||||
| chr16:72093602-72093952 | Rare:83 | ||||
| chr16:74296496-74296941 | Common:1; Rare:157 | ||||
| chr16:75433408-75433787 | Common:4; Rare:115 | ||||
| chr16:75566222-75566507 | Common:2; Rare:139 | ||||
| chr16:75647584-75647837 | Common:2; Rare:124; Clinvar:4; Clinvar (pathogenic):1 |