| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86555175-86555306 | Rare:68 | ||||
| chr16:87317337-87317517 | Common:6; Rare:70 | ||||
| chr16:87383707-87383865 | Common:1; Rare:59 | ||||
| chr16:87765900-87766055 | Common:1; Rare:63 | ||||
| chr16:87869056-87869128 | Common:1; Rare:18 | ||||
| chr16:87869238-87869293 | Rare:23 | ||||
| chr16:88570150-88570499 | Common:2; Rare:132 | ||||
| chr16:88663005-88663371 | Common:8; Rare:156 | ||||
| chr16:88706357-88706571 | Common:4; Rare:106 | ||||
| chr16:88716264-88716497 | Common:2; Rare:109; Clinvar (benign):2 | ||||
| chr16:88718031-88718178 | Common:3; Rare:64 | ||||
| chr16:88732340-88732674 | Common:2; Rare:178; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88803620-88803804 | Common:4; Rare:75 | ||||
| chr16:88811662-88811996 | Common:4; Rare:144; Clinvar (benign):1 | ||||
| chr16:88856870-88857178 | Common:4; Rare:146; Clinvar:2; Clinvar (benign):2 |