| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71895337-71895574 | Rare:81 | ||||
| chr16:72093602-72093950 | Rare:82 | ||||
| chr16:74296712-74296882 | Rare:64 | ||||
| chr16:74607080-74607197 | Rare:61 | ||||
| chr16:75306445-75306514 | Rare:11 | ||||
| chr16:75433408-75433812 | Common:4; Rare:121 | ||||
| chr16:75647614-75647776 | Common:1; Rare:86; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:79600732-79600891 | Common:1; Rare:48 | ||||
| chr16:81006832-81007255 | Common:3; Rare:139 | ||||
| chr16:84116801-84117056 | Common:3; Rare:98 | ||||
| chr16:84504616-84504861 | Common:8; Rare:105 | ||||
| chr16:85027620-85027819 | Common:1; Rare:106 | ||||
| chr16:86555188-86555306 | Rare:58 | ||||
| chr16:87317378-87317516 | Common:4; Rare:53 | ||||
| chr16:87765928-87766055 | Common:1; Rare:50 |