chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135039414150394142GA34GENIChomozygous50032151
135039466550394673ATATATAT--------7GENIChomozygous50032153
135039562950395630GA21GENIChomozygous50032155
135039579350395794CG30GENICpossibly homozygous50032157
135039583550395836AG20GENIChomozygous50032159
135039594850395952CGGT----18GENIChomozygous50032161
135039595350395954GA17GENIChomozygous50601981
135039609050396091GGAAGA14GENIChomozygous50032163
135039610750396109CG--19GENIChomozygous50032165
135039624550396246CT26GENIChomozygous50032169
135039636750396369TT--17GENIChomozygous50032171
135039639150396392GGT18GENIChomozygous50032173
135039645550396456AG24GENIChomozygous50032175
135039676950396770GA22GENIChomozygous50032177
135039694850396949TC24GENIChomozygous50032179
135039695950396960A-27GENIChomozygous50032181
135039725450397255GT22GENIChomozygous50032183
135039729550397296CCG18GENICpossibly homozygous50032185
135039761850397619AG21GENIChomozygous50032187
135039790750397908GT20GENIChomozygous50032189