| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79947544-79947810 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:80004497-80004687 | Common:3; Rare:44 | ||||
| chr6:80106413-80106696 | Common:2; Rare:93; Clinvar (pathogenic):1 | ||||
| chr6:82247704-82247933 | Common:1; Rare:77 | ||||
| chr6:83065727-83065978 | Common:1; Rare:84 | ||||
| chr6:83193193-83193389 | Common:3; Rare:63 | ||||
| chr6:85643817-85643941 | Common:2; Rare:39 | ||||
| chr6:87155243-87155629 | Rare:110 | ||||
| chr6:87329274-87329328 | Rare:13 | ||||
| chr6:87472900-87472998 | Common:1; Rare:38; Clinvar (benign):4 | ||||
| chr6:87589924-87590169 | Common:3; Rare:123; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87701491-87701745 | Common:1; Rare:85 | ||||
| chr6:87702225-87702528 | Common:1; Rare:90 | ||||
| chr6:88963531-88963657 | Rare:33 | ||||
| chr6:89117932-89118093 | Common:1; Rare:62 |