Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:35360965-35361078 | Rare:20 | ||||
chr1:42752334-42752627 | Rare:86; Clinvar:3; Clinvar (benign):5 | ||||
chr1:43164786-43165026 | Common:1; Rare:49 | ||||
chr1:44778680-44778974 | Common:1; Rare:69 | ||||
chr1:51790548-51790903 | Common:2; Rare:95 | ||||
chr1:51818094-51818242 | Rare:32 | ||||
chr1:58781603-58781954 | Rare:70 | ||||
chr1:58782020-58782417 | Common:1; Rare:104; Clinvar:1 | ||||
chr1:67831942-67832221 | Rare:61 | ||||
chr1:68123246-68123358 | Common:3; Rare:18 | ||||
chr1:70250364-70250844 | Rare:118 | ||||
chr1:71065697-71065908 | Rare:48 | ||||
chr1:77774529-77774593 | Rare:23 | ||||
chr1:77964883-77965118 | Common:3; Rare:60 | ||||
chr1:84501945-84502116 | Common:1; Rare:45 |