| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4734214-4734534 | Rare:101 | ||||
| chr16:5033928-5033964 | Rare:10 | ||||
| chr16:5071778-5071861 | Rare:39; Clinvar (benign):1 | ||||
| chr16:5097740-5098004 | Common:4; Rare:95 | ||||
| chr16:8797627-8797877 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868973-8869172 | Common:3; Rare:99 | ||||
| chr16:10580590-10580872 | Common:2; Rare:94 | ||||
| chr16:10743762-10743855 | Rare:31 | ||||
| chr16:10944332-10944619 | Common:1; Rare:87 | ||||
| chr16:11586887-11587028 | Common:1; Rare:40 | ||||
| chr16:11587161-11587313 | Common:1; Rare:35 | ||||
| chr16:11851499-11851614 | Rare:59 | ||||
| chr16:11915893-11916208 | Common:2; Rare:129 | ||||
| chr16:11976609-11976769 | Common:3; Rare:63 | ||||
| chr16:13920078-13920222 | Common:2; Rare:71; Clinvar:4; Clinvar (benign):1 |