| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30753187-30753494 | Common:1; Rare:99; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:30761841-30762343 | Common:4; Rare:144 | ||||
| chr16:30893940-30894275 | Common:5; Rare:91 | ||||
| chr16:30896506-30896624 | Common:1; Rare:33 | ||||
| chr16:30922561-30923107 | Common:1; Rare:156 | ||||
| chr16:30923113-30923157 | Rare:9 | ||||
| chr16:30923236-30923608 | Common:1; Rare:88 | ||||
| chr16:30924248-30924457 | Rare:32 | ||||
| chr16:30924608-30924942 | Common:1; Rare:75 | ||||
| chr16:30957251-30957304 | Common:2; Rare:14 | ||||
| chr16:30957632-30957765 | Common:1; Rare:41 | ||||
| chr16:30984944-30985214 | Common:1; Rare:71 | ||||
| chr16:30997284-30997414 | Common:1; Rare:32 | ||||
| chr16:31033381-31033783 | Common:1; Rare:121 | ||||
| chr16:31073726-31073855 | Rare:37 |