| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:7332684-7332957 | Common:1; Rare:87 | ||||
| chr16:8621606-8621745 | Common:1; Rare:52 | ||||
| chr16:8674367-8674701 | Common:2; Rare:112; Clinvar:2 | ||||
| chr16:8797609-8797891 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868983-8869263 | Common:4; Rare:125 | ||||
| chr16:10580581-10580732 | Rare:49 | ||||
| chr16:10580786-10580857 | Common:2; Rare:25 | ||||
| chr16:10743731-10743891 | Rare:66 | ||||
| chr16:10818600-10818697 | Common:1; Rare:30 | ||||
| chr16:10876964-10877280 | Common:1; Rare:65; Clinvar:4 | ||||
| chr16:10878589-10878940 | Rare:74 | ||||
| chr16:10944333-10944666 | Common:1; Rare:104 | ||||
| chr16:11586887-11587028 | Common:1; Rare:40 | ||||
| chr16:11587167-11587260 | Common:1; Rare:17 | ||||
| chr16:11668176-11668530 | Common:3; Rare:145 |