| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:10412164-10412212 | Rare:19 | ||||
| chr6:10412350-10412552 | Common:1; Rare:35 | ||||
| chr6:10415030-10415214 | Common:1; Rare:61 | ||||
| chr6:10419542-10419748 | Common:1; Rare:36 | ||||
| chr6:10521197-10521542 | Common:1; Rare:84 | ||||
| chr6:10555997-10556240 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:10694603-10694988 | Common:4; Rare:103 | ||||
| chr6:10722943-10723220 | Common:5; Rare:105 | ||||
| chr6:10747582-10747876 | Common:3; Rare:111 | ||||
| chr6:10838491-10838550 | Common:2; Rare:15; Clinvar:3 | ||||
| chr6:11232188-11232297 | Common:2; Rare:39 | ||||
| chr6:11232594-11232806 | Rare:48 | ||||
| chr6:12289895-12290561 | Common:2; Rare:127 | ||||
| chr6:13574449-13574639 | Common:1; Rare:50 | ||||
| chr6:13615180-13615550 | Common:2; Rare:144 |