| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1966713-1966882 | Rare:44 | ||||
| chr16:1971898-1972150 | Common:1; Rare:74 | ||||
| chr16:1975041-1975216 | Common:2; Rare:77 | ||||
| chr16:1983556-1983704 | Common:1; Rare:39 | ||||
| chr16:1992219-1992534 | Common:4; Rare:79 | ||||
| chr16:2009688-2009902 | Common:15; Rare:91 | ||||
| chr16:2047770-2048053 | Rare:139; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:2048446-2048749 | Rare:96; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr16:2155342-2155496 | Rare:49 | ||||
| chr16:2205714-2205908 | Common:4; Rare:86 | ||||
| chr16:2223528-2223677 | Rare:68 | ||||
| chr16:2267780-2267881 | Rare:34 | ||||
| chr16:2268052-2268520 | Common:5; Rare:170 | ||||
| chr16:2340777-2341199 | Common:2; Rare:109 | ||||
| chr16:2429112-2429470 | Common:2; Rare:114 |