| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689142-46689376 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:53703842-53704213 | Common:1; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:56451309-56451600 | Common:1; Rare:91 | ||||
| chr16:57185984-57186320 | Common:1; Rare:89 | ||||
| chr16:57447354-57447503 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:66934366-66934491 | Rare:47 | ||||
| chr16:67247464-67247727 | Rare:80 | ||||
| chr16:67481076-67481369 | Common:1; Rare:113 | ||||
| chr16:68023209-68023292 | Common:1; Rare:20 | ||||
| chr16:69339552-69339824 | Common:1; Rare:111; Clinvar (benign):1 | ||||
| chr16:69726548-69726852 | Common:3; Rare:69 | ||||
| chr16:70523532-70523822 | Common:3; Rare:92; Clinvar (pathogenic):1 | ||||
| chr16:75647620-75647831 | Common:2; Rare:105; Clinvar:4 | ||||
| chr16:84504613-84504866 | Common:8; Rare:113 | ||||
| chr16:85027613-85027776 | Common:1; Rare:81 |