| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20868969-20869146 | Common:2; Rare:37 | ||||
| chr16:20900219-20900873 | Common:4; Rare:156 | ||||
| chr16:21652600-21652622 | Rare:12 | ||||
| chr16:21952991-21953426 | Common:1; Rare:110; Clinvar (benign):3 | ||||
| chr16:21957245-21957483 | Rare:83; Clinvar (benign):1 | ||||
| chr16:22436914-22437106 | Rare:68 | ||||
| chr16:22437175-22437326 | Rare:45 | ||||
| chr16:22437397-22437682 | Common:2; Rare:83 | ||||
| chr16:23557327-23557458 | Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641234-23641548 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24729597-24729758 | Common:7; Rare:81 | ||||
| chr16:25015265-25015461 | Common:2; Rare:68 | ||||
| chr16:25111416-25111855 | Common:2; Rare:122 | ||||
| chr16:27268719-27268872 | Common:1; Rare:52 | ||||
| chr16:27549880-27550167 | Common:2; Rare:109 |