Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177516932-177517034 | Rare:43; Clinvar (pathogenic):1 | ||||
chr5:177600033-177600224 | Common:4; Rare:66; Clinvar (benign):5 | ||||
chr5:178204362-178204534 | Common:3; Rare:59 | ||||
chr5:179023676-179023816 | Common:2; Rare:40 | ||||
chr5:179559560-179559788 | Common:1; Rare:65 | ||||
chr5:179698686-179699092 | Common:3; Rare:132 | ||||
chr5:179806230-179806441 | Rare:63 | ||||
chr5:179806845-179807063 | Common:3; Rare:83 | ||||
chr5:179858798-179859020 | Rare:115 | ||||
chr5:180802782-180802976 | Common:8; Rare:79 | ||||
chr5:180861210-180861435 | Common:2; Rare:94 | ||||
chr5:181223118-181223309 | Rare:64 | ||||
chr5:181223597-181223732 | Common:2; Rare:31 | ||||
chr5:181243690-181243875 | Common:2; Rare:58 | ||||
chr5:181243878-181244247 | Common:8; Rare:107 |