| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58001313-58001562 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr16:58129254-58129587 | Common:4; Rare:105 | ||||
| chr16:58392761-58392889 | Common:2; Rare:39 | ||||
| chr16:58515377-58515540 | Common:3; Rare:62 | ||||
| chr16:58629751-58630155 | Common:2; Rare:111 | ||||
| chr16:58684711-58684859 | Common:1; Rare:42 | ||||
| chr16:58734208-58734430 | Common:5; Rare:63 | ||||
| chr16:65121965-65122198 | Common:1; Rare:83 | ||||
| chr16:65123976-65124168 | Common:1; Rare:21 | ||||
| chr16:65124312-65124418 | Rare:16 | ||||
| chr16:66549803-66550022 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66552445-66552676 | Rare:100 | ||||
| chr16:66751544-66751936 | Common:3; Rare:118 | ||||
| chr16:66880334-66880664 | Common:2; Rare:77 | ||||
| chr16:66934327-66934515 | Common:1; Rare:76 |