chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89962584299625843TG14GENIChomozygous116600461
89962627899626279GA23GENIChomozygous118131592
89962687199626872TC9GENIChomozygous118131593
89962829699628297TC22GENIChomozygous116600471
89962983899629839AG29GENIChomozygous116600479
89962992799629928AG22GENIChomozygous118131594
89963165499631655AT4GENIChomozygous116600481
89963322799633228CT25GENIChomozygous118131595
89963331799633318GC26GENIChomozygous118131596
89963376299633763TC20GENIChomozygous116858196
89963395599633956CT29GENIChomozygous116858198
89963404599634046AG25GENIChomozygous116858200
89963404699634047CG25GENIChomozygous116858202
89963505799635058GT17GENIChomozygous118131597
89963684699636847AG14GENIChomozygous116600485
89963736499637365AG20GENIChomozygous116600487
89963872599638726GA33GENIChomozygous116858214
89963910399639104CG28GENIChomozygous118131598
89963915899639159CG24GENIChomozygous116600489
89963993999639940TC7GENIChomozygous116600493
89964015199640152AG16GENIChomozygous116858218
89964092899640929GA28GENIChomozygous116858220
89964165599641656AG24GENIChomozygous116858222
89964217099642171GC21GENIChomozygous116858224
89964251599642516GC29GENIChomozygous116858228
89964265799642658TC23GENIChomozygous116858230
89964280899642809GA29GENIChomozygous116858232
89964360999643610CT22GENIChomozygous116858235