| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19555462-19555729 | Common:1; Rare:121 | ||||
| chr16:19718432-19718574 | Rare:55 | ||||
| chr16:20741727-20741978 | Common:1; Rare:113 | ||||
| chr16:20763947-20764021 | Common:1; Rare:12 | ||||
| chr16:20806331-20806677 | Rare:107 | ||||
| chr16:20900226-20900892 | Common:4; Rare:156 | ||||
| chr16:21158498-21158718 | Common:2; Rare:63 | ||||
| chr16:21599364-21599748 | Common:4; Rare:132 | ||||
| chr16:21952986-21953422 | Common:1; Rare:110; Clinvar (benign):3 | ||||
| chr16:21957257-21957566 | Rare:104; Clinvar (benign):1 | ||||
| chr16:22206014-22206344 | Common:1; Rare:89 | ||||
| chr16:22436928-22437071 | Rare:54 | ||||
| chr16:22437075-22437313 | Rare:80 | ||||
| chr16:22437427-22437678 | Common:2; Rare:66 | ||||
| chr16:23452724-23452857 | Rare:49; Clinvar (benign):1 |