chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578908655789094CTCTCTCT--------11GENIChomozygous757315052
135578919955789201TC--12GENICheterozygous757315054
135578922755789228TTC11GENIChomozygous757315055
135578923655789237GGTC11GENICheterozygous757315056
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC10GENIChomozygous757315057
135578942255789423CG7GENICpossibly homozygous650338187
135578965455789656TC--15GENICheterozygous757315058
135578972455789725TTC9GENIChomozygous757315059
135578973155789732CCTCT10GENIChomozygous757315060
135579103355791034GA23GENIChomozygous650338188
135579200955792010GGCACA9GENICpossibly homozygous757315062
135579200955792010GGCACACA9GENICheterozygous757315063
135579303055793031AG18GENIChomozygous650338189
135579307355793074T-15GENIChomozygous757315064
135579400355794004GA11GENIChomozygous650338190
135579446155794462CT24GENIChomozygous650338191
135579512755795128AG18GENIChomozygous650338192
135579527055795271CT24GENIChomozygous650338193
135579548355795484TC26GENIChomozygous650338194
135579568655795687GGC18GENIChomozygous757315065
135579722655797248ACACACACACACACACACACAC----------------------5GENICheterozygous757315066
135579722855797248ACACACACACACACACACAC--------------------5GENICheterozygous757315067
135579807855798079AACACCC1GENIChomozygous757315071
135579808655798087AG6GENIChomozygous650338195
135579830955798310TTG15GENIChomozygous757315073
135579838855798389AAGACTGACTGACTGACT7GENIChomozygous757315075
135579909955799100AC26GENIChomozygous650338196
135579987755799878AG23GENIChomozygous650338197
135580062355800624CG15GENIChomozygous650338198
135580164955801650AG24GENIChomozygous650338199
135580172555801726AG25GENIChomozygous650338200