| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:23453154-23453258 | Rare:30 | ||||
| chr16:23557336-23557452 | Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641247-23641550 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:24539312-24539586 | Common:1; Rare:87 | ||||
| chr16:24729611-24729727 | Common:6; Rare:66 | ||||
| chr16:25111537-25111797 | Common:2; Rare:67 | ||||
| chr16:27268724-27268872 | Common:1; Rare:50 | ||||
| chr16:27549892-27550167 | Common:2; Rare:101 | ||||
| chr16:28711372-28711514 | |||||
| chr16:28822579-28822729 | Rare:55 | ||||
| chr16:28824286-28824501 | Common:2; Rare:76 | ||||
| chr16:28846265-28846715 | Common:2; Rare:147; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:28863735-28863875 | Common:1; Rare:38 | ||||
| chr16:28925167-28925272 | Rare:29 | ||||
| chr16:28974667-28974792 | Rare:57 |