| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:519863-520167 | Rare:91 | ||||
| chr16:2603309-2603472 | Common:1; Rare:66 | ||||
| chr16:2673339-2673673 | Common:10; Rare:117 | ||||
| chr16:3106629-3106795 | Common:2; Rare:62 | ||||
| chr16:4253781-4253987 | Common:3; Rare:75 | ||||
| chr16:4307532-4307834 | Common:3; Rare:112 | ||||
| chr16:12041686-12041882 | Common:1; Rare:58 | ||||
| chr16:13110120-13110298 | Common:1; Rare:47 | ||||
| chr16:14824696-14824932 | Common:1; Rare:24 | ||||
| chr16:20348231-20348463 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:21820398-21820433 | Rare:8 | ||||
| chr16:21820435-21820477 | Rare:12 | ||||
| chr16:25107082-25107187 | Rare:26 | ||||
| chr16:25148921-25148945 | Rare:8 | ||||
| chr16:28902470-28902626 | Rare:41; Clinvar:1; Clinvar (benign):2 |