| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:234465-234531 | Rare:29 | ||||
| chr16:234725-234853 | Rare:53 | ||||
| chr16:381924-382131 | Common:6; Rare:79 | ||||
| chr16:401724-401945 | Common:1; Rare:91 | ||||
| chr16:636225-636456 | Common:4; Rare:72 | ||||
| chr16:684303-684475 | Common:3; Rare:94 | ||||
| chr16:714879-715171 | Common:4; Rare:108 | ||||
| chr16:720507-720599 | Rare:23 | ||||
| chr16:721130-721203 | Common:1; Rare:23 | ||||
| chr16:726874-727126 | Common:4; Rare:66 | ||||
| chr16:1351813-1351971 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:1474997-1475073 | Common:1; Rare:29; Clinvar:1 | ||||
| chr16:1493271-1493591 | Common:4; Rare:98 | ||||
| chr16:1533481-1533697 | Common:1; Rare:40 | ||||
| chr16:1612029-1612360 | Common:2; Rare:110; Clinvar:1 |