| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149546001-149546120 | Rare:50 | ||||
| chr6:149566235-149566421 | Common:1; Rare:58 | ||||
| chr6:149648478-149648843 | Common:2; Rare:90 | ||||
| chr6:149718059-149718153 | Common:1; Rare:31 | ||||
| chr6:149746479-149746642 | Common:2; Rare:78 | ||||
| chr6:149749652-149749865 | Rare:105 | ||||
| chr6:151240240-151240252 | Rare:3 | ||||
| chr6:151325475-151325720 | Common:2; Rare:61 | ||||
| chr6:151452029-151452548 | Common:4; Rare:183 | ||||
| chr6:152302007-152302240 | Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152636147-152636288 | Common:1; Rare:35 | ||||
| chr6:152983022-152983343 | Common:2; Rare:99 | ||||
| chr6:152983499-152983768 | Common:4; Rare:103 | ||||
| chr6:153002447-153002895 | Common:7; Rare:180 | ||||
| chr6:154039224-154039636 | Common:8; Rare:152 |