| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169270255-169270700 | Common:2; Rare:96 | ||||
| chr4:169270872-169271056 | Common:1; Rare:58 | ||||
| chr4:169271092-169271392 | Common:2; Rare:73 | ||||
| chr4:169271603-169271687 | Common:2; Rare:16 | ||||
| chr4:169612129-169612261 | Rare:20 | ||||
| chr4:169612483-169612835 | Common:7; Rare:106; Clinvar:5; Clinvar (benign):2 | ||||
| chr4:169620087-169620685 | Common:2; Rare:191 | ||||
| chr4:169757787-169758080 | Common:2; Rare:97 | ||||
| chr4:170026337-170026647 | Common:4; Rare:129 | ||||
| chr4:173168172-173168324 | Common:2; Rare:36 | ||||
| chr4:173168444-173168893 | Common:4; Rare:123 | ||||
| chr4:173169066-173169207 | Common:1; Rare:44 | ||||
| chr4:173333754-173334065 | Common:1; Rare:76 | ||||
| chr4:173334242-173334933 | Rare:175 | ||||
| chr4:173335071-173335396 | Common:2; Rare:81 |