| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:21599390-21599712 | Common:4; Rare:116 | ||||
| chr16:21953028-21953419 | Common:1; Rare:99; Clinvar (benign):3 | ||||
| chr16:22007982-22008374 | Common:2; Rare:118 | ||||
| chr16:22436905-22437037 | Rare:44 | ||||
| chr16:22437097-22437313 | Rare:71 | ||||
| chr16:23452734-23452808 | Rare:27 | ||||
| chr16:23453127-23453250 | Rare:35 | ||||
| chr16:23557294-23557473 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23641247-23641545 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24539323-24539601 | Common:1; Rare:96 | ||||
| chr16:24729604-24729745 | Common:6; Rare:74 | ||||
| chr16:25111458-25111894 | Common:2; Rare:135 | ||||
| chr16:25257464-25257571 | Rare:37 | ||||
| chr16:25258320-25258375 | Common:2; Rare:34 | ||||
| chr16:27268719-27268877 | Common:1; Rare:55 |