chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1235188152235188153CT24GENIChomozygous61610104
1235188762235188763TTAC10GENICheterozygous61683633
1235188762235188763TTACAC10GENICheterozygous61610105
1235189204235189205GC13GENIChomozygous61610106
1235192220235192221CG21GENIChomozygous61610107
1235192689235192690AG23GENIChomozygous61610108
1235192976235192977TC24GENIChomozygous61610109
1235195179235195180CT17GENIChomozygous61610110
1235195551235195552TA18GENIChomozygous61610111
1235195846235195847T-16GENIChomozygous61610112
1235195860235195861A-14GENIChomozygous61610113
1235196631235196632CA21GENIChomozygous61610114
1235196966235196967AT10GENIChomozygous61610115
1235197943235197947TGTG----9GENIChomozygous61610116
1235198745235198746CA6GENIChomozygous61610117
1235199168235199169AAG17GENIChomozygous61610118
1235199602235199603CCA24GENIChomozygous61610119
1235199605235199606T-12GENICpossibly homozygous61323022
1235199756235199757AAC24GENIChomozygous61610120
1235200019235200020AG21GENIChomozygous61610121
1235200130235200131GA14GENIChomozygous61610122