| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:10385925-10386067 | Rare:53 | ||||
| chr16:10743740-10743861 | Rare:45 | ||||
| chr16:10744065-10744306 | Common:1; Rare:87 | ||||
| chr16:10877004-10877313 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:10944369-10944630 | Common:1; Rare:80 | ||||
| chr16:11586917-11587018 | Common:1; Rare:33 | ||||
| chr16:11668195-11668489 | Common:3; Rare:128 | ||||
| chr16:11687977-11688244 | Common:1; Rare:55 | ||||
| chr16:11797160-11797527 | Common:3; Rare:142 | ||||
| chr16:11851517-11851653 | Rare:66 | ||||
| chr16:11915900-11916272 | Common:2; Rare:147 | ||||
| chr16:11964914-11965240 | Common:4; Rare:70 | ||||
| chr16:11976615-11976766 | Common:2; Rare:57 | ||||
| chr16:12803524-12803950 | Common:8; Rare:154 | ||||
| chr16:14071024-14071344 | Common:3; Rare:104 |