| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74296676-74296882 | Rare:80 | ||||
| chr16:74666807-74667177 | Common:8; Rare:129 | ||||
| chr16:75433379-75433812 | Common:4; Rare:136 | ||||
| chr16:75464646-75464777 | Common:1; Rare:41 | ||||
| chr16:75623229-75623370 | Common:3; Rare:48 | ||||
| chr16:75647607-75647794 | Common:1; Rare:94; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:81006786-81007273 | Common:5; Rare:166 | ||||
| chr16:83953092-83953240 | Rare:43 | ||||
| chr16:84116806-84117097 | Common:3; Rare:120 | ||||
| chr16:84699843-84700020 | Common:2; Rare:80 | ||||
| chr16:85799287-85799762 | Common:3; Rare:153 | ||||
| chr16:86555190-86555308 | Rare:58 | ||||
| chr16:87317393-87317516 | Common:2; Rare:45 | ||||
| chr16:87765901-87766044 | Rare:56 | ||||
| chr16:88570174-88570416 | Common:1; Rare:87 |