| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85449470-85449727 | Common:2; Rare:56 | ||||
| chr6:85449905-85450182 | Common:1; Rare:85 | ||||
| chr6:85593706-85593946 | Common:1; Rare:88 | ||||
| chr6:85642803-85643011 | Common:1; Rare:83 | ||||
| chr6:85643296-85643441 | Rare:64 | ||||
| chr6:85643817-85643968 | Common:2; Rare:45 | ||||
| chr6:86937602-86937766 | Common:1; Rare:38 | ||||
| chr6:87155262-87155637 | Rare:110 | ||||
| chr6:87344745-87344821 | Rare:8 | ||||
| chr6:87407916-87408087 | Common:3; Rare:37 | ||||
| chr6:87472703-87472742 | Common:1; Rare:8 | ||||
| chr6:87472862-87473006 | Common:1; Rare:51; Clinvar (benign):4 | ||||
| chr6:87589896-87590192 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87702164-87702487 | Common:3; Rare:103 | ||||
| chr6:88047659-88047923 | Common:2; Rare:83 |