| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:10992912-10993057 | Common:1; Rare:41 | ||||
| chr16:19116332-19116595 | Common:2; Rare:40 | ||||
| chr16:19717465-19717497 | Rare:5 | ||||
| chr16:28239726-28239794 | Rare:11 | ||||
| chr16:29816480-29816521 | Rare:15 | ||||
| chr16:29819405-29819634 | Common:3; Rare:62 | ||||
| chr16:29845858-29846282 | Common:2; Rare:124 | ||||
| chr16:30875325-30875465 | Rare:46 | ||||
| chr16:31191429-31191775 | Common:1; Rare:141; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:31474387-31474698 | Rare:99 | ||||
| chr16:55509697-55509975 | Common:3; Rare:51 | ||||
| chr16:67079542-67079673 | Rare:16 | ||||
| chr16:70674296-70674315 | Rare:4 | ||||
| chr16:72664938-72665191 | Common:1; Rare:83 | ||||
| chr16:86483635-86483653 | Common:1; Rare:1 |