| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:82247709-82248018 | Common:1; Rare:98 | ||||
| chr6:82363485-82363714 | Common:1; Rare:63 | ||||
| chr6:82364144-82364303 | Common:2; Rare:41 | ||||
| chr6:83068018-83068116 | Common:1; Rare:23 | ||||
| chr6:83193201-83193397 | Common:3; Rare:68 | ||||
| chr6:85449888-85450175 | Common:1; Rare:87 | ||||
| chr6:85593761-85593927 | Common:1; Rare:57 | ||||
| chr6:85643817-85643933 | Common:2; Rare:37 | ||||
| chr6:87155268-87155615 | Rare:97 | ||||
| chr6:87472900-87473004 | Common:1; Rare:40; Clinvar (benign):4 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702203-87702514 | Common:1; Rare:97 | ||||
| chr6:88963555-88963830 | Common:2; Rare:93 | ||||
| chr6:89638714-89638824 | Common:3; Rare:41 | ||||
| chr6:89819709-89819917 | Rare:68 |