Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:176388569-176388859 | Common:4; Rare:115 | ||||
chr5:176549204-176549377 | Rare:41 | ||||
chr5:177022642-177022732 | Rare:30 | ||||
chr5:177133488-177133794 | Rare:111 | ||||
chr5:177371046-177371123 | Common:17; Rare:86 | ||||
chr5:177516908-177517079 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:177600029-177600183 | Common:3; Rare:51; Clinvar (benign):2 | ||||
chr5:179623631-179623980 | Common:4; Rare:123 | ||||
chr5:179698610-179699091 | Common:4; Rare:170 | ||||
chr5:179820669-179820921 | Common:6; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr5:179858797-179859047 | Rare:133 | ||||
chr5:180861367-180861598 | Common:2; Rare:64 | ||||
chr5:181261081-181261223 | Rare:43 | ||||
chr6:693054-693194 | Rare:47 | ||||
chr6:2245436-2245831 | Common:1; Rare:134 |