| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5003649-5003843 | Common:5; Rare:61 | ||||
| chr6:5003999-5004102 | Common:2; Rare:52 | ||||
| chr6:5260677-5261017 | Common:3; Rare:116; Clinvar (benign):4 | ||||
| chr6:5261238-5261558 | Common:9; Rare:81 | ||||
| chr6:6588617-6588773 | Common:1; Rare:52 | ||||
| chr6:7107458-7107839 | Common:1; Rare:127 | ||||
| chr6:7108206-7108670 | Common:1; Rare:146 | ||||
| chr6:7313042-7313383 | Common:5; Rare:126 | ||||
| chr6:7389740-7389976 | Common:1; Rare:61 | ||||
| chr6:7541409-7541694 | Rare:87; Clinvar (benign):1 | ||||
| chr6:7910606-7910902 | Common:4; Rare:116 | ||||
| chr6:8064332-8064632 | Common:4; Rare:88 | ||||
| chr6:8435440-8435702 | Common:6; Rare:94 | ||||
| chr6:10694636-10694994 | Common:4; Rare:91 | ||||
| chr6:10722817-10723237 | Common:6; Rare:142 |