| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32853654-32853819 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32853979-32854227 | Common:2; Rare:60 | ||||
| chr6:32940946-32941184 | Common:1; Rare:47 | ||||
| chr6:32968483-32968616 | Common:2; Rare:38 | ||||
| chr6:32968812-32968933 | Common:4; Rare:39 | ||||
| chr6:32977418-32978004 | Common:4; Rare:201; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:33009565-33009847 | Common:3; Rare:55 | ||||
| chr6:33200384-33200437 | Rare:11 | ||||
| chr6:33200639-33200925 | Common:2; Rare:86 | ||||
| chr6:33201066-33201260 | Rare:38 | ||||
| chr6:33201557-33201807 | Common:2; Rare:56 | ||||
| chr6:33202101-33202327 | Common:2; Rare:72 | ||||
| chr6:33202374-33202676 | Rare:70 | ||||
| chr6:33204996-33205305 | Common:3; Rare:97 | ||||
| chr6:33208443-33208560 | Rare:32 |