chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148516388185163882TC26GENICpossibly homozygous49020798
148516405385164054GC7GENICheterozygous49020799
148516475885164759GT18GENIChomozygous49020800
148516506485165065AG20GENICpossibly homozygous49020801
148516542785165428TA2GENIChomozygous49020803
148516561285165613TC3GENICheterozygous48812532
148516616085166161TC17GENIChomozygous49020805
148516625285166378CATCCACTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTGCTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTT------------------------------------------------------------------------------------------------------------------------------9GENICpossibly homozygous49292223
148516712185167122CT18GENICpossibly homozygous49020807
148516717985167180CT19GENIChomozygous49020808
148516786485167865AG5GENIChomozygous49020809
148516790185167903AG--6GENIChomozygous49020810
148516846485168465TC10GENIChomozygous49020811
148516856485168565GA23GENIChomozygous49020812
148516901985169020GA8GENICpossibly homozygous49020813
148517038585170386AG11GENICheterozygous49020814
148517097585170976TC17GENICpossibly homozygous49020815
148517119785171198AG5GENICheterozygous49020816
148517137585171376AG7GENIChomozygous49020817
148517378385173784TC6GENIChomozygous49020818
148517411585174116CCT7GENICheterozygous49020820
148517449585174496TTG8GENIChomozygous49431469
148517449685174497TTG9GENIChomozygous49431470
148517580785175808AT9GENIChomozygous49020822
148517652685176527GA3GENIChomozygous49020823
148517968985179690CT8GENICpossibly homozygous49020826
148517983185179832G-7GENICpossibly homozygous49020827
148517983485179835GC7GENICpossibly homozygous49431471
148517985985179860AT21GENIChomozygous49020828
148518097985180980AC17GENICheterozygous49020829
148518184085181841CT7GENICheterozygous49523184