| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5071782-5071852 | Rare:33; Clinvar (benign):1 | ||||
| chr16:5097728-5097989 | Common:4; Rare:97 | ||||
| chr16:8720427-8720776 | Common:2; Rare:98 | ||||
| chr16:8797610-8797877 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868968-8869175 | Common:3; Rare:102 | ||||
| chr16:10385833-10386089 | Rare:91 | ||||
| chr16:10580563-10580783 | Rare:69 | ||||
| chr16:10580796-10580867 | Common:2; Rare:25 | ||||
| chr16:10743563-10743880 | Common:1; Rare:109 | ||||
| chr16:10944327-10944643 | Common:1; Rare:99 | ||||
| chr16:11586900-11587018 | Common:1; Rare:39 | ||||
| chr16:11668248-11668489 | Common:3; Rare:110 | ||||
| chr16:11742853-11743077 | Common:2; Rare:93 | ||||
| chr16:11797146-11797557 | Common:4; Rare:158 | ||||
| chr16:11851484-11851645 | Common:1; Rare:83 |