Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:77020289-77020670 | Rare:95 | ||||
chr4:77075965-77076120 | Common:3; Rare:79 | ||||
chr4:77862650-77862879 | Common:3; Rare:88 | ||||
chr4:78057441-78057619 | Common:2; Rare:38 | ||||
chr4:78551591-78551843 | Rare:63 | ||||
chr4:78939181-78939530 | Common:2; Rare:146 | ||||
chr4:80072617-80072739 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr4:81154200-81154324 | Common:1; Rare:44 | ||||
chr4:81471798-81472067 | Common:1; Rare:84 | ||||
chr4:82373932-82374186 | Common:2; Rare:76 | ||||
chr4:82429367-82429634 | Common:1; Rare:164; Clinvar:13; Clinvar (benign):5 | ||||
chr4:82430731-82430825 | Rare:42 | ||||
chr4:82890973-82891299 | Common:1; Rare:118 | ||||
chr4:82900449-82900805 | Common:1; Rare:113 | ||||
chr4:82900879-82901023 | Rare:58 |