chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136780802567808026CT19GENIChomozygous66076601
136780867367808674CT10GENIChomozygous66076604
136780893867808939CT33GENIChomozygous66076607
136780962067809621TC12GENIChomozygous66076610
136780991067809911AG9GENIChomozygous66076613
136781009467810095GA18GENIChomozygous66076615
136781228567812285ATT5GENIChomozygous66868078
136781358667813587TC21GENIChomozygous66076627
136781465867814665CCCTGTC8GENICheterozygous66868081
136781539567815396A10GENIChomozygous66868085
136781738667817386T22GENICheterozygous66868088
136781876167818762CG22GENIChomozygous66076633
136782257667822577TC17GENIChomozygous66076636
136782273767822738TC24GENIChomozygous66076639
136782299567822996AG24GENIChomozygous66076641
136782304667823047AC22GENIChomozygous66076644
136782304767823048GT22GENIChomozygous66076647
136782524567825246AT10GENIChomozygous66076650
136782574767825748GA13GENIChomozygous66076653
136782604967826050GA24GENIChomozygous66076656
136782650767826508AG21GENIChomozygous66076659
136782689967826900AT25GENIChomozygous66076662
136782868367828684TC22GENIChomozygous66076664
136782945667829457GA12GENIChomozygous66076667
136782976967829770CA29GENIChomozygous66076670
136783005967830060CT16GENIChomozygous66076673
136783152967831530AG30GENIChomozygous66076676
136783208567832086CA17GENIChomozygous66076679
136783270167832702GT9GENIChomozygous66076682
136783270367832704GT9GENIChomozygous66076685