| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:228916-229192 | Common:2; Rare:132 | ||||
| chr16:234688-234864 | Common:1; Rare:82 | ||||
| chr16:254000-254106 | Common:1; Rare:14 | ||||
| chr16:282883-283241 | Common:13; Rare:104 | ||||
| chr16:376779-377048 | Common:3; Rare:78 | ||||
| chr16:396988-397312 | Common:8; Rare:79 | ||||
| chr16:401713-401968 | Common:2; Rare:109 | ||||
| chr16:636244-636478 | Common:4; Rare:66 | ||||
| chr16:641736-641950 | Common:3; Rare:71 | ||||
| chr16:642095-642456 | Common:1; Rare:119 | ||||
| chr16:649252-649404 | Common:1; Rare:54 | ||||
| chr16:671710-671927 | Common:2; Rare:121 | ||||
| chr16:680324-680472 | Common:2; Rare:49 | ||||
| chr16:681149-681557 | Rare:130; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr16:684326-684475 | Common:3; Rare:81 |