| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70289350-70289900 | Common:25; Rare:1108; Clinvar:7; Clinvar (benign):15 | ||||
| chr16:70299093-70299519 | Common:4; Rare:223 | ||||
| chr16:70346660-70347020 | Common:9; Rare:637 | ||||
| chr16:70438208-70438995 | Common:15; Rare:464 | ||||
| chr16:70438958-70439600 | Common:10; Rare:859 | ||||
| chr16:70453741-70454757 | Common:19; Rare:826 | ||||
| chr16:70454783-70455183 | Common:4; Rare:99 | ||||
| chr16:70523061-70523461 | Common:8; Rare:192; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:70523391-70523906 | Common:21; Rare:909; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr16:70524000-70524200 | Common:2; Rare:70 | ||||
| chr16:70524268-70524668 | Common:6; Rare:105 | ||||
| chr16:70579710-70580030 | Common:1; Rare:73 | ||||
| chr16:70653640-70654240 | Common:2; Rare:241 | ||||
| chr16:70685341-70685796 | Common:5; Rare:159 | ||||
| chr16:70685740-70685940 | Common:1; Rare:58 |