| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68311379-68311475 | Rare:10 | ||||
| chr16:68529971-68530194 | Common:6; Rare:110 | ||||
| chr16:68539144-68539361 | Common:2; Rare:102 | ||||
| chr16:68539491-68539633 | Common:2; Rare:55 | ||||
| chr16:68539639-68539773 | Common:2; Rare:58 | ||||
| chr16:68539813-68539906 | Common:1; Rare:43 | ||||
| chr16:68644431-68644659 | Rare:49 | ||||
| chr16:68644677-68644811 | Common:1; Rare:32; Clinvar:5; Clinvar (benign):1 | ||||
| chr16:68644818-68644970 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr16:68645087-68645374 | Common:1; Rare:97; Clinvar:8 | ||||
| chr16:68645575-68645837 | Common:1; Rare:87; Clinvar:2 | ||||
| chr16:68645864-68646107 | Common:2; Rare:55 | ||||
| chr16:68843495-68843787 | Rare:102 | ||||
| chr16:68843918-68844175 | Rare:45 | ||||
| chr16:69106128-69106319 | Common:2; Rare:50 |