chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107615509276155093GA21GENIChomozygous116640753
107615653076156531AG29GENIChomozygous116640757
107615661976156620CA18GENIChomozygous116640759
107615668676156687AG21GENIChomozygous116640761
107615673376156734TC25GENIChomozygous116640763
107615700076157001AG20GENICheterozygous118001850
107616208376162084TG24GENIChomozygous116801092
107616281776162818AG11GENIChomozygous116640769
107616623476166235AG26GENIChomozygous116640779
107616735076167351TA22GENIChomozygous116801094
107616784976167850TG13GENICheterozygous118068409
107616816276168163AG19GENIChomozygous116640783
107616851576168516TA27GENIChomozygous116801096
107616917576169176GA24GENIChomozygous116801098
107617166776171668TC24GENIChomozygous116640789
107617207876172079CT12GENIChomozygous118001852
107617496576174966AG18GENICheterozygous117086198
107617496976174970AG17GENICheterozygous118044216
107617711576177116GA24GENIChomozygous116801100
107617802476178025AG19GENIChomozygous116640809
107617845576178456TC16GENIChomozygous116640813
107618053676180537CA22GENICpossibly homozygous116801102
107618076576180766AG23GENIChomozygous116640815
107618150776181508AC17GENIChomozygous116640819
107618185876181859AG15GENIChomozygous116640821
107618242576182426GA23GENIChomozygous116801104
107618271076182711CT19GENIChomozygous116801106
107618279876182799AG29GENIChomozygous116801108