chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1255120316255120317T-5GENIChomozygous61325942
1255121318255121319CA1GENIChomozygous61325944
1255121378255121379A-2GENIChomozygous61166060
1255121344255121345GA1GENIChomozygous62557818
1255122021255122022AG20GENIChomozygous61166062
1255122822255122823GA18GENIChomozygous61166064
1255123782255123783TC25GENIChomozygous61166065
1255124206255124207CT22GENIChomozygous61325945
1255124429255124430AAACAC11GENIChomozygous61166066
1255124477255124478CCT17GENIChomozygous61166067
1255124486255124487AAC19GENIChomozygous61166069
1255125188255125189GA10GENIChomozygous61325947
1255125300255125301CG18GENIChomozygous61166070
1255125338255125339CCGTGT4GENIChomozygous61325948
1255126727255126728GT20GENIChomozygous61166072
1255128042255128043AG18GENIChomozygous61166073
1255128214255128215TC20GENIChomozygous61166076
1255128233255128234C-18GENIChomozygous61325949
1255129164255129169CTCTC-----7GENIChomozygous61325950
1255129196255129200CTCC----6GENIChomozygous61166077
1255129680255129684TGTG----1GENIChomozygous62315876
1255128079255128080A-12GENIChomozygous62241565
1255124479255124480GC18GENIChomozygous62211495