| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46763268-46763439 | Rare:34 | ||||
| chr16:46789926-46790066 | Common:4; Rare:29 | ||||
| chr16:46831096-46831328 | Common:2; Rare:88 | ||||
| chr16:46973577-46973796 | Rare:98 | ||||
| chr16:47460965-47461383 | Common:2; Rare:172; Clinvar (benign):2 | ||||
| chr16:48244253-48244566 | Common:2; Rare:94 | ||||
| chr16:48365885-48366097 | Common:5; Rare:63 | ||||
| chr16:48385268-48385561 | Common:3; Rare:116 | ||||
| chr16:50066283-50066481 | Common:3; Rare:103 | ||||
| chr16:53099155-53099180 | Rare:4 | ||||
| chr16:53208321-53208583 | Rare:48 | ||||
| chr16:53703809-53704206 | Common:1; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286407-54286505 | Rare:25 | ||||
| chr16:54286681-54287030 | Common:2; Rare:102 | ||||
| chr16:54930554-54930748 | Common:1; Rare:51 |