| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88856861-88857163 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217627-89217738 | Common:1; Rare:49 | ||||
| chr16:89508289-89508455 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560537-89560717 | Rare:75 | ||||
| chr16:89657644-89658091 | Common:3; Rare:235 | ||||
| chr16:89686574-89686704 | Common:6; Rare:59 | ||||
| chr16:89720865-89721081 | Common:2; Rare:68 | ||||
| chr16:89873482-89873856 | Common:3; Rare:168 | ||||
| chr16:89923171-89923368 | Rare:81 | ||||
| chr16:89948560-89948803 | Common:3; Rare:72 | ||||
| chr16:89972455-89972627 | Common:1; Rare:63 | ||||
| chr17:732301-732611 | Common:2; Rare:107 | ||||
| chr17:752146-752311 | Common:2; Rare:68 | ||||
| chr17:1516578-1516945 | Common:1; Rare:126 | ||||
| chr17:1645693-1646031 | Common:2; Rare:82 |