| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58630293-58630687 | Common:1; Rare:96 | ||||
| chr16:58684675-58684845 | Rare:44 | ||||
| chr16:58734215-58734449 | Common:5; Rare:70 | ||||
| chr16:66516819-66517146 | Rare:57 | ||||
| chr16:66549619-66549763 | Common:2; Rare:38 | ||||
| chr16:66549777-66549992 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66550068-66550152 | Common:2; Rare:47; Clinvar (benign):2 | ||||
| chr16:66552391-66552656 | Rare:106 | ||||
| chr16:66604533-66604756 | Rare:66 | ||||
| chr16:66751536-66751927 | Common:3; Rare:124 | ||||
| chr16:66830195-66830525 | Rare:50 | ||||
| chr16:66830836-66831125 | Rare:122 | ||||
| chr16:66873198-66873361 | Rare:40 | ||||
| chr16:66880173-66880651 | Common:3; Rare:105 | ||||
| chr16:66880723-66880876 | Common:2; Rare:38 |