| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132490-69132671 | Rare:67 | ||||
| chr16:69187050-69187181 | Rare:49 | ||||
| chr16:69339548-69339841 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr16:69424489-69424698 | Common:1; Rare:63 | ||||
| chr16:69565715-69566015 | Common:4; Rare:123 | ||||
| chr16:69566219-69566341 | Common:1; Rare:33 | ||||
| chr16:69726547-69726752 | Common:3; Rare:46 | ||||
| chr16:69762282-69762385 | Rare:23 | ||||
| chr16:70114124-70114393 | Common:3; Rare:97 | ||||
| chr16:70258110-70258348 | Rare:70; Clinvar:6; Clinvar (benign):3 | ||||
| chr16:70289446-70289649 | Rare:74; Clinvar:1 | ||||
| chr16:70346804-70347008 | Common:2; Rare:102 | ||||
| chr16:70523539-70523837 | Common:3; Rare:92 | ||||
| chr16:70579776-70580044 | Rare:60 | ||||
| chr16:70678357-70678748 | Common:5; Rare:93 |