| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41072475-41072888 | Rare:118 | ||||
| chr6:41921104-41921192 | Rare:22 | ||||
| chr6:42142611-42142714 | Common:1; Rare:32 | ||||
| chr6:42217844-42217987 | Common:3; Rare:37 | ||||
| chr6:42879577-42879940 | Rare:106 | ||||
| chr6:42929209-42929566 | Common:4; Rare:104 | ||||
| chr6:42984280-42984619 | Rare:85 | ||||
| chr6:43013869-43014270 | Common:2; Rare:87 | ||||
| chr6:43516873-43517109 | Common:4; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575957-43576153 | Rare:74 | ||||
| chr6:43687768-43687838 | Common:1; Rare:30 | ||||
| chr6:43771912-43771980 | Rare:14 | ||||
| chr6:44127351-44127665 | Common:4; Rare:91 | ||||
| chr6:44219589-44219641 | Rare:14 | ||||
| chr6:49463167-49463430 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 |