| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30699006-30699402 | Rare:104; Clinvar (benign):1 | ||||
| chr16:30762053-30762364 | Common:3; Rare:99 | ||||
| chr16:30768781-30769250 | Rare:147 | ||||
| chr16:30894036-30894281 | Common:3; Rare:63 | ||||
| chr16:30922567-30922890 | Common:1; Rare:92 | ||||
| chr16:30923236-30923601 | Common:1; Rare:87 | ||||
| chr16:30948775-30949140 | Rare:71 | ||||
| chr16:30956968-30957314 | Common:3; Rare:78 | ||||
| chr16:31033303-31033628 | Common:2; Rare:109 | ||||
| chr16:31073718-31073837 | Rare:37 | ||||
| chr16:31074199-31074457 | Common:1; Rare:72 | ||||
| chr16:31179828-31180227 | Common:3; Rare:175; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31188818-31189074 | Common:1; Rare:56 | ||||
| chr16:31189643-31190412 | Common:2; Rare:215; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:31190783-31191169 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 |