| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29805343-29805758 | Common:2; Rare:196 | ||||
| chr16:29863121-29863555 | Common:1; Rare:110 | ||||
| chr16:29996070-29996259 | Common:2; Rare:65 | ||||
| chr16:30069564-30070018 | Common:1; Rare:169; Clinvar:6; Clinvar (benign):7 | ||||
| chr16:30355219-30355460 | Common:2; Rare:84 | ||||
| chr16:30896465-30896641 | Common:1; Rare:42 | ||||
| chr16:31471925-31472189 | Rare:59 | ||||
| chr16:46689131-46689313 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689516-46689694 | Common:2; Rare:72; Clinvar (benign):2 | ||||
| chr16:47461051-47461350 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr16:53703836-53704216 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:56451299-56451606 | Common:1; Rare:102 | ||||
| chr16:56608521-56608803 | Common:2; Rare:81 | ||||
| chr16:57185985-57186333 | Common:1; Rare:99 | ||||
| chr16:57447354-57447517 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):1 |