| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28593242-28593466 | Common:4; Rare:121 | ||||
| chr16:28605887-28606257 | Common:10; Rare:141 | ||||
| chr16:28606765-28607079 | Common:2; Rare:130 | ||||
| chr16:28843084-28843447 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:28864645-28864818 | Rare:35 | ||||
| chr16:29074950-29075017 | Rare:28 | ||||
| chr16:29290883-29291198 | Common:3; Rare:65 | ||||
| chr16:29594484-29594872 | Common:5; Rare:92 | ||||
| chr16:29595039-29595104 | Common:4; Rare:38 | ||||
| chr16:29595295-29595662 | Common:3; Rare:156 | ||||
| chr16:29760722-29760931 | Rare:24 | ||||
| chr16:29824895-29825138 | Rare:45 | ||||
| chr16:29841741-29842091 | Rare:114 | ||||
| chr16:30334770-30334952 | Common:1; Rare:54 | ||||
| chr16:30335287-30335529 | Common:2; Rare:90 |