| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30762052-30762348 | Common:3; Rare:94 | ||||
| chr16:30787139-30787272 | Rare:18 | ||||
| chr16:30893884-30894275 | Common:5; Rare:102 | ||||
| chr16:30923068-30923103 | Rare:13 | ||||
| chr16:30923242-30923608 | Common:1; Rare:88 | ||||
| chr16:31033456-31033581 | Common:1; Rare:49 | ||||
| chr16:31074184-31074450 | Common:1; Rare:73 | ||||
| chr16:31108333-31108465 | Rare:34 | ||||
| chr16:31179827-31180168 | Common:2; Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:31442745-31443059 | Common:1; Rare:52 | ||||
| chr16:31458905-31459161 | Rare:75 | ||||
| chr16:31459288-31459510 | Common:1; Rare:93 | ||||
| chr16:31487767-31488048 | Common:1; Rare:83; Clinvar:1 | ||||
| chr16:31508182-31508516 | Common:5; Rare:148 | ||||
| chr16:31873653-31873931 | Common:1; Rare:93 |