| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43770063-43770230 | Common:3; Rare:50 | ||||
| chr6:44126185-44126502 | Common:1; Rare:61 | ||||
| chr6:44126799-44126952 | Rare:44 | ||||
| chr6:44127272-44127707 | Common:4; Rare:121 | ||||
| chr6:44219560-44219645 | Rare:22 | ||||
| chr6:44247749-44247819 | Rare:28 | ||||
| chr6:44297688-44297811 | Common:1; Rare:46 | ||||
| chr6:44387407-44387747 | Common:4; Rare:84 | ||||
| chr6:46129793-46130173 | Common:5; Rare:122 | ||||
| chr6:46170931-46171214 | Common:1; Rare:70 | ||||
| chr6:46921858-46922089 | Common:2; Rare:64 | ||||
| chr6:47478067-47478260 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:49463161-49463430 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995266-52995812 | Common:4; Rare:227 | ||||
| chr6:53348926-53349211 | Common:2; Rare:91 |