| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074160-31074456 | Common:2; Rare:85 | ||||
| chr16:31094542-31094881 | Common:1; Rare:116; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108292-31108477 | Rare:44 | ||||
| chr16:31179818-31180242 | Common:3; Rare:187; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31183856-31184396 | Common:1; Rare:178; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:31190036-31190399 | Common:1; Rare:98; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:31459324-31459517 | Common:1; Rare:79 | ||||
| chr16:31471950-31472194 | Rare:58 | ||||
| chr16:31507812-31508028 | Common:1; Rare:75 | ||||
| chr16:31508356-31508493 | Common:4; Rare:59 | ||||
| chr16:32253703-32253964 | Common:3; Rare:98 | ||||
| chr16:46689111-46689310 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689500-46689773 | Common:2; Rare:120; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46959000-46959335 | Rare:95 | ||||
| chr16:46973615-46973789 | Rare:81 |