chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96754706667547067TC55GENICpossibly homozygous117551872
96754711767547118GA49GENIChomozygous117551874
96754714567547146GA50GENIChomozygous117551876
96754719667547197GA48GENIChomozygous117551878
96754733467547335CT70GENIChomozygous117551880
96754743567547436CT80GENIChomozygous117551883
96754760367547604AC68GENIChomozygous117551885
96754780267547803AG73GENICpossibly homozygous117551887
96754844867548449AG87GENIChomozygous117551889
96754846267548463AG83GENICpossibly homozygous117551891
96754868767548688TC51GENICpossibly homozygous117551893
96754869567548696CT46GENICpossibly homozygous117551895
96754870567548706TC40GENICpossibly homozygous117551897
96754871167548712TC38GENICpossibly homozygous117551899
96754892267548923AC66GENIChomozygous117551901
96754897867548979AT58GENICpossibly homozygous117551903
96754916667549167TA57GENICpossibly homozygous117551905
96754956367549564TA61GENIChomozygous117551907
96755081367550814AG69GENIChomozygous117551909
96755095767550958CT59GENIChomozygous117551911
96755100167551002AG58GENIChomozygous117551913
96755109267551093CT63GENICpossibly homozygous117551915
96755141167551412AG55GENIChomozygous117551917
96755227367552274TC55GENIChomozygous117551919
96755356567553566CT42GENIChomozygous117551921
96755373767553738AG55GENIChomozygous117551923
96755396567553966AG43GENIChomozygous117551925
96755419467554195TG67GENIChomozygous117551927
96755486467554865GA68GENIChomozygous117551929
96755493967554940AG59GENIChomozygous117551931
96755555667555557AG24GENIChomozygous117551933
96755580167555802CA47GENICheterozygous117551935
96755583467555835GA45GENICheterozygous117551937
96755620967556210TG51GENIChomozygous117551939
96755708667557087GA85GENIChomozygous117551941
96755722267557223GC59GENIChomozygous117551943
96755748367557484GA69GENIChomozygous117551945
96755775367557754GA73GENIChomozygous117551947
96755950767559508GC64GENICpossibly homozygous117551949
96756515067565151TG60GENICheterozygous117551951