| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136550346-136550687 | Common:2; Rare:103 | ||||
| chr6:137219111-137219220 | Common:1; Rare:34 | ||||
| chr6:138107127-138107237 | Rare:35 | ||||
| chr6:138404058-138404274 | Common:1; Rare:63 | ||||
| chr6:138405739-138406018 | Rare:43 | ||||
| chr6:138499368-138499614 | Common:2; Rare:46 | ||||
| chr6:138773646-138773813 | Common:3; Rare:77 | ||||
| chr6:139028640-139028882 | Common:1; Rare:51 | ||||
| chr6:142147140-142147284 | Rare:51 | ||||
| chr6:142301734-142302179 | Common:8; Rare:126 | ||||
| chr6:143060688-143060992 | Common:8; Rare:112 | ||||
| chr6:143450666-143450971 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511132-143511313 | Rare:33 | ||||
| chr6:143511651-143511792 | Common:4; Rare:35 | ||||
| chr6:143843196-143843479 | Common:2; Rare:96 |