| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:73048646-73048719 | Common:1; Rare:21 | ||||
| chr16:73058760-73058913 | Rare:44 | ||||
| chr16:73058916-73059035 | Common:1; Rare:23 | ||||
| chr16:74296400-74296465 | Rare:15 | ||||
| chr16:74296629-74297123 | Common:3; Rare:184 | ||||
| chr16:74606347-74606885 | Common:2; Rare:197 | ||||
| chr16:74607005-74607285 | Rare:143 | ||||
| chr16:74665991-74666084 | Common:2; Rare:36 | ||||
| chr16:74666781-74667278 | Common:8; Rare:150 | ||||
| chr16:74700483-74700687 | Common:1; Rare:50 | ||||
| chr16:74774779-74775024 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:74984555-74984616 | Rare:18 | ||||
| chr16:74984661-74984720 | Rare:13 | ||||
| chr16:74984763-74984957 | Rare:60 | ||||
| chr16:74985015-74985372 | Common:2; Rare:117 |