| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1771499-1771852 | Common:3; Rare:138 | ||||
| chr16:1782510-1783009 | Common:4; Rare:165 | ||||
| chr16:1943176-1943513 | Common:1; Rare:105 | ||||
| chr16:1959421-1959671 | Common:5; Rare:114 | ||||
| chr16:1964824-1965061 | Common:6; Rare:102 | ||||
| chr16:1971798-1972140 | Common:3; Rare:104 | ||||
| chr16:2009703-2009949 | Common:14; Rare:101 | ||||
| chr16:2047782-2048038 | Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155670-2155810 | Common:1; Rare:44 | ||||
| chr16:2223304-2223666 | Rare:146 | ||||
| chr16:2429125-2429467 | Common:2; Rare:109 | ||||
| chr16:2459980-2460123 | Rare:37 | ||||
| chr16:2682372-2682608 | Rare:104 | ||||
| chr16:2777001-2777392 | Common:2; Rare:144 | ||||
| chr16:2980410-2980619 | Common:2; Rare:73 |