chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4171772847171772848C50GENIChomozygous128104787
4171772854171772854G51GENIChomozygous128104788
4171772857171772857C52GENIChomozygous128104789
4171772984171772984G49GENIChomozygous128104790
4171773045171773045AACAG44GENIChomozygous128104791
4171785380171785381T40GENIChomozygous128104792
4171789500171789500CCTGTG52GENIChomozygous128104793
4171793645171793679AAGCATGACAAGGTAGGAAGTGCCTTGCTTGGAG32GENIChomozygous128104794
4171802434171802435C46GENIChomozygous128104795
4171802475171802476A41GENIChomozygous128104796
4171808362171808416CGCACACACGCACGCGCGCGCGCGCGCGCACACACACACGCACGCGCGCGCGCG31GENICheterozygous128104797
4171820550171820551A19GENIChomozygous128104802
4171820564171820566GC20GENIChomozygous128104803
4171820585171820586T22GENIChomozygous128104804
4171820600171820600C23GENIChomozygous128104805
4171820622171820623T21GENIChomozygous128104806
4171820637171820638G18GENIChomozygous128104807
4171820643171820643C19GENIChomozygous128104808
4171820649171820650C16GENIChomozygous128104809
4171820668171820668C14GENIChomozygous128104810
4171820797171820797T9GENIChomozygous128104811
4171820813171820814T10GENIChomozygous128104812
4171820858171820858C16GENIChomozygous128104813
4171820868171820868C21GENIChomozygous128104814
4171820877171820878TA21GENIChomozygous119283200
4171820878171820879AC21GENIChomozygous113067950
4171820882171820883AC20GENIChomozygous112952033