chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48869512488695125AG5GENIChomozygous113282600
48869745088697451AT9GENIChomozygous112773077
48869758288697583GA12GENIChomozygous113282601
48869792188697922AC10GENIChomozygous112773078
48869806188698062GA14GENIChomozygous112773079
48869825488698255AG6GENICheterozygous112773080
48869906788699068CT19GENIChomozygous112773081
48869944888699449GA17GENICpossibly homozygous112773082
48869974588699746TA14GENIChomozygous112773083
48870049088700491GA11GENIChomozygous112773084
48870051088700511CT13GENIChomozygous112773085
48870120588701206AC21GENIChomozygous112773087
48870190888701909GA20GENIChomozygous113282602
48870198888701989CT9GENICheterozygous113282603
48870347788703478AC19GENIChomozygous112773090
48870514688705147AC18GENIChomozygous112773091
48870618588706186GA34GENIChomozygous113131302
48870849188708492TC13GENIChomozygous112773097
48870961388709614AG5GENIChomozygous112773099
48871501488715015TG10GENICheterozygous113131308
48871655788716558GA23GENIChomozygous112773113
48871863388718634TC30GENIChomozygous113282608
48871902488719025GC15GENIChomozygous112773121
48871975588719756AG20GENIChomozygous112773129
48872124388721244GT11GENICheterozygous112773134