| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75284628-75285022 | Common:1; Rare:124 | ||||
| chr6:75601770-75601899 | Rare:49 | ||||
| chr6:75749047-75749281 | Common:5; Rare:80; Clinvar:2 | ||||
| chr6:78867481-78867600 | Rare:56 | ||||
| chr6:79078273-79078586 | Common:1; Rare:126 | ||||
| chr6:79234585-79234866 | Common:3; Rare:71 | ||||
| chr6:79537355-79537665 | Common:2; Rare:97; Clinvar:4 | ||||
| chr6:83065743-83065981 | Common:1; Rare:78 | ||||
| chr6:83193222-83193397 | Common:3; Rare:64 | ||||
| chr6:85449912-85450140 | Common:1; Rare:68 | ||||
| chr6:85593786-85594109 | Common:1; Rare:92 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155237-87155582 | Rare:89 | ||||
| chr6:87472832-87472997 | Common:1; Rare:57; Clinvar (benign):4 | ||||
| chr6:87589920-87590163 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 |