| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46973577-46973781 | Rare:87 | ||||
| chr16:47460965-47461378 | Common:2; Rare:170; Clinvar (benign):2 | ||||
| chr16:48244495-48244508 | Rare:3 | ||||
| chr16:48609965-48610277 | Common:2; Rare:112 | ||||
| chr16:50245937-50246184 | Common:2; Rare:58 | ||||
| chr16:50266422-50266595 | Common:1; Rare:50 | ||||
| chr16:53098912-53099222 | Rare:61 | ||||
| chr16:53099601-53099750 | Rare:30 | ||||
| chr16:53703814-53704187 | Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286765-54287016 | Common:1; Rare:76 | ||||
| chr16:55479009-55479214 | Common:1; Rare:48 | ||||
| chr16:55479585-55479630 | Rare:9 | ||||
| chr16:56451298-56451605 | Common:1; Rare:101 | ||||
| chr16:56608308-56608716 | Common:4; Rare:119 | ||||
| chr16:56682352-56682504 | Common:3; Rare:58 |