| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20763903-20764069 | Common:2; Rare:26 | ||||
| chr16:20806331-20806659 | Rare:103 | ||||
| chr16:20900226-20900873 | Common:4; Rare:154 | ||||
| chr16:21233594-21233843 | Common:1; Rare:65 | ||||
| chr16:21652602-21652735 | Rare:31 | ||||
| chr16:21952975-21953478 | Common:1; Rare:129; Clinvar (benign):3 | ||||
| chr16:22206547-22206592 | Rare:12 | ||||
| chr16:22436940-22437326 | Rare:137 | ||||
| chr16:22437338-22437391 | Rare:8 | ||||
| chr16:22437441-22437696 | Common:2; Rare:68 | ||||
| chr16:22814794-22814889 | Rare:40 | ||||
| chr16:23452529-23452808 | Rare:67 | ||||
| chr16:23453127-23453217 | Rare:28 | ||||
| chr16:23557315-23557557 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641219-23641530 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 |