| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:164977578-164977727 | Rare:42 | ||||
| chr4:165112818-165113015 | Common:1; Rare:57 | ||||
| chr4:165327411-165327741 | Common:2; Rare:95 | ||||
| chr4:168480399-168480444 | Rare:7 | ||||
| chr4:168480452-168480522 | Common:1; Rare:16 | ||||
| chr4:168496921-168497206 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:168631587-168631810 | Rare:61 | ||||
| chr4:169010227-169010456 | Common:1; Rare:67 | ||||
| chr4:169270939-169271162 | Common:1; Rare:75 | ||||
| chr4:169612333-169612397 | Rare:12; Clinvar:1 | ||||
| chr4:169620385-169620725 | Common:2; Rare:117 | ||||
| chr4:169660040-169660325 | Common:1; Rare:52 | ||||
| chr4:173333498-173333883 | Common:2; Rare:99 | ||||
| chr4:173334280-173334740 | Rare:117 | ||||
| chr4:173369732-173369941 | Common:1; Rare:67 |