| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074634-31074916 | Common:3; Rare:56 | ||||
| chr16:31094523-31094817 | Common:1; Rare:110; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108333-31108633 | Rare:64 | ||||
| chr16:31117880-31118104 | Rare:57 | ||||
| chr16:31179820-31180211 | Common:3; Rare:170; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180583-31180744 | Common:2; Rare:65 | ||||
| chr16:31184736-31185068 | Common:4; Rare:111; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr16:31442745-31443061 | Common:1; Rare:52 | ||||
| chr16:31459297-31459510 | Common:1; Rare:87 | ||||
| chr16:31508351-31508516 | Common:4; Rare:72 | ||||
| chr16:31713082-31713367 | Common:1; Rare:70 | ||||
| chr16:46689115-46689425 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689466-46689714 | Common:2; Rare:93; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46831101-46831325 | Common:2; Rare:86 | ||||
| chr16:46973555-46973820 | Rare:116 |