Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177006324-177006499 | Rare:51 | ||||
chr5:177022600-177022756 | Common:1; Rare:65 | ||||
chr5:177133463-177133800 | Rare:121 | ||||
chr5:177303683-177304075 | Common:3; Rare:146 | ||||
chr5:177311869-177312046 | Common:1; Rare:52 | ||||
chr5:177351643-177351953 | Rare:80 | ||||
chr5:177497545-177497864 | Common:1; Rare:118 | ||||
chr5:177516906-177517093 | Common:1; Rare:71; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:178153813-178154110 | Rare:90; Clinvar:5; Clinvar (benign):1 | ||||
chr5:178204320-178204534 | Common:3; Rare:75 | ||||
chr5:179678372-179678656 | Common:3; Rare:108 | ||||
chr5:179698580-179699092 | Common:4; Rare:180 | ||||
chr5:179806321-179806448 | Rare:41 | ||||
chr5:179806614-179806793 | Common:2; Rare:47 | ||||
chr5:179806865-179807094 | Common:3; Rare:86 |