| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68023187-68023349 | Common:2; Rare:50 | ||||
| chr16:68084508-68084821 | Rare:60 | ||||
| chr16:68085108-68085367 | Common:2; Rare:45 | ||||
| chr16:68237625-68237877 | Rare:69 | ||||
| chr16:68245161-68245424 | Common:1; Rare:79 | ||||
| chr16:68264320-68264764 | Rare:126 | ||||
| chr16:68310855-68311152 | Common:4; Rare:147 | ||||
| chr16:68448651-68448863 | Common:1; Rare:52 | ||||
| chr16:68529978-68530146 | Common:5; Rare:85 | ||||
| chr16:68539145-68539327 | Common:2; Rare:92 | ||||
| chr16:69026461-69026583 | Rare:29 | ||||
| chr16:69132498-69132703 | Rare:73 | ||||
| chr16:69187045-69187181 | Rare:52 | ||||
| chr16:69187321-69187569 | Common:1; Rare:46 | ||||
| chr16:69329042-69329395 | Common:1; Rare:142; Clinvar (benign):1 |