| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:15257180-15257278 | Rare:12 | ||||
| chr16:15300451-15300730 | Common:2; Rare:22 | ||||
| chr16:15464619-15464905 | Rare:46 | ||||
| chr16:15520974-15521024 | Rare:11 | ||||
| chr16:15719583-15719822 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):3 | ||||
| chr16:15732688-15732769 | Rare:19 | ||||
| chr16:15747565-15747996 | Common:3; Rare:109; Clinvar:10; Clinvar (benign):6 | ||||
| chr16:15750277-15750614 | Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr16:15757833-15758131 | Rare:88; Clinvar:4; Clinvar (benign):10 | ||||
| chr16:15953620-15953675 | Common:1; Rare:13 | ||||
| chr16:16104227-16104604 | Common:4; Rare:117 | ||||
| chr16:16144068-16144171 | Common:2; Rare:24 | ||||
| chr16:16455504-16455641 | Rare:11 | ||||
| chr16:17392232-17392493 | Rare:48 | ||||
| chr16:17961902-17962139 | Common:3; Rare:70 |