chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2114745357114745358CT8GENIChomozygous564677309
2114745405114745406AG31GENICpossibly homozygous563618174
2114745513114745514CT19GENIChomozygous563618175
2114745930114745931TC12GENIChomozygous563618176
2114745953114745954TC8GENICheterozygous563618177
2114747143114747144TA8GENIChomozygous563618178
2114747169114747172TTT---2GENIChomozygous708053551
2114747537114747538CT20GENICpossibly homozygous563618179
2114747680114747681GA16GENIChomozygous563618180
2114748669114748670CT12GENICheterozygous564677310
2114749309114749310TA23GENIChomozygous563618181
2114749643114749644AG14GENICpossibly homozygous563618182
2114750211114750212TG19GENIChomozygous563618183
2114750661114750662AC18GENIChomozygous563618184
2114750738114750739AC10GENIChomozygous563618185
2114750739114750740GA9GENIChomozygous564677311
2114750940114750941AG16GENIChomozygous563618186
2114751124114751125CT20GENICpossibly homozygous563618187
2114751682114751683TC15GENICpossibly homozygous563618188
2114751777114751778CG11GENIChomozygous563618189
2114752163114752164AG13GENICpossibly homozygous563618190
2114752297114752298AG19GENICpossibly homozygous563618191
2114752355114752356CG23GENIChomozygous563618192
2114752802114752803TC15GENIChomozygous563618193
2114753270114753271TC7GENICpossibly homozygous563618194
2114753307114753308CG6GENIChomozygous563618195
2114753354114753355CT23GENICpossibly homozygous563618196
2114753694114753695CT14GENICpossibly homozygous563618197