| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46747882-46748507 | Rare:164 | ||||
| chr16:46789915-46790089 | Common:4; Rare:44 | ||||
| chr16:46973559-46973781 | Rare:93 | ||||
| chr16:47461031-47461383 | Common:2; Rare:138; Clinvar (benign):2 | ||||
| chr16:48244260-48244538 | Common:2; Rare:85 | ||||
| chr16:48385258-48385549 | Common:3; Rare:113 | ||||
| chr16:49281771-49282062 | Common:2; Rare:89 | ||||
| chr16:53434364-53434527 | Common:1; Rare:59 | ||||
| chr16:53504406-53504521 | Common:1; Rare:15 | ||||
| chr16:53703809-53704215 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286665-54287089 | Common:3; Rare:121 | ||||
| chr16:55479037-55479211 | Rare:42 | ||||
| chr16:56451296-56451619 | Common:1; Rare:108 | ||||
| chr16:56608276-56608694 | Common:3; Rare:118 | ||||
| chr16:56625618-56625845 | Rare:72 |