| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69754805-69755173 | Common:2; Rare:256 | ||||
| chr16:69762135-69762689 | Common:7; Rare:358 | ||||
| chr16:70114054-70114430 | Common:9; Rare:325 | ||||
| chr16:70114566-70114710 | Common:3; Rare:41 | ||||
| chr16:70251811-70251986 | Common:1; Rare:156 | ||||
| chr16:70289298-70289831 | Common:13; Rare:517; Clinvar:3; Clinvar (benign):11 | ||||
| chr16:70299068-70299292 | Common:2; Rare:89 | ||||
| chr16:70299270-70299850 | Common:4; Rare:222 | ||||
| chr16:70346089-70346633 | Common:2; Rare:157 | ||||
| chr16:70346692-70347010 | Common:5; Rare:385 | ||||
| chr16:70453830-70454240 | Common:1; Rare:99 | ||||
| chr16:70454335-70454744 | Common:9; Rare:294 | ||||
| chr16:70523161-70523324 | Common:2; Rare:38 | ||||
| chr16:70523439-70523904 | Common:9; Rare:446; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr16:70524093-70524869 | Common:12; Rare:262 |