chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1254751166254751167CT19GENIChomozygous61632815
1254751935254751936AC15GENIChomozygous61325834
1254751958254751959CT9GENIChomozygous61325835
1254751962254751963CT9GENIChomozygous61325836
1254753805254753806AC19GENICpossibly homozygous61165515
1254753917254753918CT8GENIChomozygous61165516
1254754442254754443T-4GENIChomozygous61165518
1254754611254754612TA20GENICpossibly homozygous61165520
1254754780254754781TA14GENIChomozygous62304659
1254754808254754814CAGCAG------1GENIChomozygous61165521
1254755818254755819CA5GENIChomozygous61165523
1254755819254755820CG5GENIChomozygous61165524
1254757075254757076GT15GENICpossibly homozygous61165527
1254758749254758750CG11GENICpossibly homozygous61165530
1254759930254759931CT12GENIChomozygous62304660
1254760113254760114AG3GENIChomozygous61165539
1254760225254760226CT14GENICpossibly homozygous62304661
1254760934254760935TC10GENIChomozygous61165542
1254760958254760959AAT1GENIChomozygous61165543
1254761123254761124GA24GENICpossibly homozygous62304662
1254763017254763018GA10GENICheterozygous61632824
1254763023254763024GA7GENICpossibly homozygous61165548