| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56729949-56730192 | Common:1; Rare:59 | ||||
| chr16:56781677-56781866 | Common:1; Rare:32 | ||||
| chr16:56931909-56932160 | Common:3; Rare:121 | ||||
| chr16:56989554-56989594 | Rare:9 | ||||
| chr16:57185823-57186382 | Common:3; Rare:162 | ||||
| chr16:57244938-57245262 | Common:3; Rare:110 | ||||
| chr16:57447360-57447511 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57479749-57479947 | Common:1; Rare:35 | ||||
| chr16:57619935-57620106 | Rare:37 | ||||
| chr16:57639283-57639591 | Common:2; Rare:60; Clinvar (pathogenic):1 | ||||
| chr16:58001343-58001456 | Rare:39 | ||||
| chr16:58129260-58129581 | Common:4; Rare:103 | ||||
| chr16:58249854-58250012 | Rare:42 | ||||
| chr16:58629751-58630139 | Common:2; Rare:106 | ||||
| chr16:58684708-58684816 | Rare:34 |