| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67719260-67719440 | Rare:46 | ||||
| chr16:67806511-67806872 | Rare:81 | ||||
| chr16:67828495-67828770 | Rare:91 | ||||
| chr16:67846587-67846983 | Common:2; Rare:114 | ||||
| chr16:67935630-67935954 | Common:1; Rare:106 | ||||
| chr16:67936799-67937020 | Common:1; Rare:32 | ||||
| chr16:67968568-67968863 | Common:2; Rare:99 | ||||
| chr16:68023209-68023325 | Common:1; Rare:31 | ||||
| chr16:68085154-68085367 | Common:2; Rare:36 | ||||
| chr16:68234019-68234477 | Rare:115 | ||||
| chr16:68245161-68245417 | Common:1; Rare:76 | ||||
| chr16:68310913-68311089 | Common:1; Rare:90 | ||||
| chr16:68529987-68530142 | Common:4; Rare:78 | ||||
| chr16:68645563-68645719 | Rare:51; Clinvar:2 | ||||
| chr16:68811577-68811821 | Common:1; Rare:63; Clinvar:18; Clinvar (benign):16 |