| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:13486034-13486434 | Common:11; Rare:92 | ||||
| chr6:13487537-13487931 | Common:3; Rare:93 | ||||
| chr6:13574378-13574629 | Common:2; Rare:60 | ||||
| chr6:13615115-13615413 | Common:4; Rare:129 | ||||
| chr6:13711833-13711999 | Common:1; Rare:71 | ||||
| chr6:13712020-13712334 | Common:2; Rare:100 | ||||
| chr6:13814153-13814309 | Common:1; Rare:64 | ||||
| chr6:13814406-13814729 | Common:3; Rare:114 | ||||
| chr6:13924067-13924467 | Common:6; Rare:172 | ||||
| chr6:13924650-13925020 | Common:1; Rare:119 | ||||
| chr6:14117400-14117820 | Common:3; Rare:139 | ||||
| chr6:15245727-15246016 | Common:1; Rare:71 | ||||
| chr6:15248564-15248877 | Common:3; Rare:136 | ||||
| chr6:15662770-15663270 | Common:2; Rare:185; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:16238481-16238703 | Common:3; Rare:82 |