chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1134828787134828787G35GENIChomozygous127433064
1134860739134860740CG32GENIChomozygous108236837
1134860743134860744TG34GENIChomozygous108236839
1134860745134860746AT34GENIChomozygous108236841
1134860750134860751AT33GENIChomozygous108236843
1134860905134860906AT4GENIChomozygous108236845
1134860907134860915AGAAGGAT4GENIChomozygous130212848
1134861038134861038C22GENIChomozygous127433078
1134861050134861050T25GENIChomozygous127433079
1134861094134861095G30GENIChomozygous127433080
1134861116134861116T27GENIChomozygous127433081
1134861127134861127C21GENIChomozygous127433082
1134861134134861135T21GENIChomozygous127433083
1134861144134861145A17GENIChomozygous127433084
1134861177134861178A12GENIChomozygous127433085
1134861237134861238C18GENIChomozygous127433086
1134861283134861287AAAC33GENICpossibly homozygous127433087
1134862751134862752CT24GENIChomozygous108236857
1134865084134865085G67GENIChomozygous127433089
1134865117134865117A66GENIChomozygous127433090
1134865135134865135A62GENIChomozygous127433091
1134865172134865172T54GENIChomozygous127433092
1134865187134865187T57GENIChomozygous127433093
1134865263134865263A64GENIChomozygous127433094
1134865345134865346G53GENIChomozygous127433095
1134865355134865355C20GENICpossibly homozygous130212849
1134865448134865449TA43GENIChomozygous108236865
1134865529134865530G42GENIChomozygous127433099
1134865538134865539A42GENIChomozygous127433100
1134865599134865600G55GENIChomozygous127433101
1134865648134865648A58GENIChomozygous127433102
1134865651134865652T60GENIChomozygous127433103
1134865655134865656TG60GENIChomozygous120473493
1134865656134865657GA60GENIChomozygous120473494