| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:50368706-50369158 | Common:7; Rare:157 | ||||
| chr16:50548225-50548501 | Common:2; Rare:105 | ||||
| chr16:50693534-50693672 | Rare:51 | ||||
| chr16:50696703-50696944 | Rare:45 | ||||
| chr16:50697091-50697212 | Common:2; Rare:29; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:50741634-50742245 | Common:7; Rare:188; Clinvar:1 | ||||
| chr16:50742247-50742459 | Common:3; Rare:58 | ||||
| chr16:50742662-50742775 | Rare:22 | ||||
| chr16:50742946-50743018 | Rare:11 | ||||
| chr16:53054792-53055312 | Common:3; Rare:112 | ||||
| chr16:53055368-53055478 | Rare:19 | ||||
| chr16:53099103-53099196 | Rare:20 | ||||
| chr16:53099561-53099848 | Rare:55 | ||||
| chr16:53130352-53130691 | Common:4; Rare:81 | ||||
| chr16:53130722-53130978 | Common:2; Rare:86 |