| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21957259-21957566 | Rare:104; Clinvar (benign):1 | ||||
| chr16:22206541-22206577 | Rare:8 | ||||
| chr16:22436949-22437086 | Rare:52 | ||||
| chr16:22437166-22437326 | Rare:49 | ||||
| chr16:22437455-22437485 | Rare:9 | ||||
| chr16:22437513-22437676 | Common:2; Rare:40 | ||||
| chr16:23557336-23557557 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641206-23641551 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24539326-24539637 | Common:2; Rare:109 | ||||
| chr16:24540392-24540438 | Rare:13 | ||||
| chr16:24729611-24729745 | Common:6; Rare:72 | ||||
| chr16:25015259-25015461 | Common:2; Rare:69 | ||||
| chr16:25111521-25111797 | Common:2; Rare:76 | ||||
| chr16:27268713-27268872 | Common:1; Rare:57 | ||||
| chr16:27313286-27313611 | Common:2; Rare:62 |