| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:50681268-50681406 | Common:1; Rare:30 | ||||
| chr16:50693505-50693619 | Rare:46 | ||||
| chr16:50741674-50742162 | Common:7; Rare:147; Clinvar:1 | ||||
| chr16:50742727-50742782 | Rare:10 | ||||
| chr16:53054803-53055048 | Common:2; Rare:58 | ||||
| chr16:53099601-53099779 | Rare:38 | ||||
| chr16:53503223-53503557 | Common:9; Rare:102 | ||||
| chr16:53703809-53704213 | Common:1; Rare:129; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286744-54287016 | Common:1; Rare:85 | ||||
| chr16:55478716-55478918 | Common:1; Rare:35 | ||||
| chr16:55479026-55479211 | Common:1; Rare:44 | ||||
| chr16:55479504-55479630 | Rare:42; Clinvar:2 | ||||
| chr16:56451287-56451619 | Common:1; Rare:111 | ||||
| chr16:56519973-56520217 | Common:7; Rare:91; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56607143-56607731 | Common:2; Rare:113 |