| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1361567-1361817 | Common:1; Rare:106; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:1532444-1532699 | Rare:49 | ||||
| chr16:1537109-1537277 | Common:2; Rare:49 | ||||
| chr16:1904648-1904857 | Common:2; Rare:38 | ||||
| chr16:2037538-2037839 | Common:3; Rare:113 | ||||
| chr16:2281118-2281443 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:2281451-2281747 | Rare:82 | ||||
| chr16:2284979-2285235 | Common:5; Rare:59 | ||||
| chr16:2317217-2317365 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr16:2330604-2330717 | Common:1; Rare:16 | ||||
| chr16:2339752-2339855 | Rare:19 | ||||
| chr16:2603405-2603477 | Rare:35 | ||||
| chr16:2673302-2673708 | Common:10; Rare:145 | ||||
| chr16:3020929-3021315 | Rare:118 | ||||
| chr16:3021496-3021626 | Rare:49 |