| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69339510-69339830 | Common:1; Rare:144; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69726448-69726806 | Common:3; Rare:91 | ||||
| chr16:70289440-70289653 | Rare:76; Clinvar:1 | ||||
| chr16:70346781-70346935 | Common:1; Rare:76 | ||||
| chr16:70454470-70454604 | Common:1; Rare:42 | ||||
| chr16:70523500-70523883 | Common:3; Rare:132; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:72008531-72008775 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr16:72093539-72093950 | Rare:106 | ||||
| chr16:74296874-74296902 | Rare:17 | ||||
| chr16:74666851-74667087 | Common:1; Rare:81 | ||||
| chr16:75647590-75647864 | Common:4; Rare:137; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190680-77191004 | Common:12; Rare:105 | ||||
| chr16:77191157-77191231 | Common:1; Rare:33 | ||||
| chr16:81006416-81006533 | Rare:31 | ||||
| chr16:81006805-81007251 | Common:4; Rare:152 |