| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56451287-56451605 | Common:1; Rare:104 | ||||
| chr16:56505972-56506137 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:56608414-56608665 | Common:2; Rare:73 | ||||
| chr16:56625626-56625826 | Rare:63 | ||||
| chr16:56632492-56632667 | Common:1; Rare:49 | ||||
| chr16:56638509-56638669 | Common:1; Rare:65 | ||||
| chr16:56657586-56657730 | Rare:35 | ||||
| chr16:56729974-56730189 | Common:1; Rare:49 | ||||
| chr16:56931975-56932185 | Common:2; Rare:120 | ||||
| chr16:56932798-56933077 | Common:2; Rare:49 | ||||
| chr16:56989350-56989616 | Common:1; Rare:61; Clinvar:1 | ||||
| chr16:57025217-57025501 | Common:3; Rare:76 | ||||
| chr16:57041860-57042000 | Common:1; Rare:30 | ||||
| chr16:57185291-57185491 | Rare:44 | ||||
| chr16:57185804-57186382 | Common:3; Rare:164 |