chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75328787053287871AG34GENIChomozygous53924937
75328803353288034TC36GENIChomozygous53924939
75329103653291037AG48GENIChomozygous54653028
75329106953291070TC45GENIChomozygous54653030
75329147953291480GGGTGT6GENIChomozygous54653032
75329451753294518CCA29GENIChomozygous54195693
75329479253294793GA33GENIChomozygous54653034
75329593453295935AG32GENIChomozygous53924944
75329888253298883GA37GENIChomozygous54653040
75329678353296784GA27GENIChomozygous54653036
75329863453298635TC20GENIChomozygous54653038
75329914653299147CCAT27GENIChomozygous54653042
75330189053301891GT33GENIChomozygous54653044
75330214353302147AAAT----27GENIChomozygous54653046
75330420853304210TG--30GENIChomozygous53924949
75330426053304261GA50GENIChomozygous54653048
75330643953306440T-29GENIChomozygous54195695
75330675353306754AC30GENIChomozygous54653050
75331001953310020GA25GENIChomozygous53924952
75331184253311843CT24GENIChomozygous54653052
75331193753311938AG26GENIChomozygous54653054
75331274953312750CT29GENIChomozygous54653056
75331327453313275CG37GENIChomozygous53924953
75331350753313508TTGC54GENIChomozygous53924957
75331538053315381CCA18GENICpossibly homozygous54653058
75331615853316159AG35GENIChomozygous53924958
75331757953317580T-18GENIChomozygous54653060
75331822053318221GT41GENIChomozygous54653062
75331866753318668TA12GENIChomozygous53924960
75332215353322154GA35GENIChomozygous53924967
75332221953322220CT38GENIChomozygous53924969
75332223053322231GA36GENIChomozygous53924971
75332236453322365GA31GENIChomozygous53924973
75332241153322412TA27GENIChomozygous53924975
75332259653322597GGT21GENIChomozygous53924977
75332355653323557CA43GENIChomozygous53924982
75332483553324836GA22GENIChomozygous54653064
75332514953325150CCCCT27GENIChomozygous53924987
75332560753325608AG41GENIChomozygous53924991
75332727053327271GA22GENIChomozygous54653066