chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242959982242959983CT62GENIChomozygous135851769
1242960234242960235G57GENIChomozygous135469569
1242963395242963396AC68GENIChomozygous135851770
1242964999242965000GC34GENIChomozygous135851771
1242966962242966963GA56GENIChomozygous135851772
1242967394242967395CT40GENIChomozygous135851773
1242968720242968721TC47GENIChomozygous135851774
1242970616242970617GA59GENIChomozygous135851775
1242971696242971708ATACACATACAC47GENIChomozygous135469570
1242972636242972637AG43GENIChomozygous135851776
1242972810242972811GA59GENICpossibly homozygous135851777
1242973774242973775TC63GENIChomozygous135851778
1242975992242975993CA64GENICpossibly homozygous135851779
1242978739242978740AG30GENIChomozygous135851780
1242978767242978768GA28GENIChomozygous135851781
1242978767242978768G28GENICheterozygous402983517
1242964999242965000G34GENICheterozygous402983515
1242971707242971708CT47GENICheterozygous153920250
1242971707242971708C47GENIChomozygous402983516
1242978877242978878AC48GENIChomozygous135851782
1242978922242978923GC45GENIChomozygous135851783
1242979353242979353A53GENIChomozygous135469571
1242979514242979515GT27GENICpossibly homozygous135851784
1242980124242980125CT46GENIChomozygous135851785
1242980705242980706CT59GENIChomozygous135851786
1242980858242980859A25GENICpossibly homozygous135469572
1242983774242983775TA52GENIChomozygous135851787
1242984885242984886GA44GENIChomozygous135851788
1242985071242985072TC59GENIChomozygous135851789
1242986954242986955AG25GENIChomozygous135851790
1242987949242987950CG44GENIChomozygous135851791
1242988349242988350TC60GENIChomozygous135851792
1242989549242989550AG54GENIChomozygous135851793
1242990302242990303GA68GENIChomozygous135851794
1242991967242991968AG62GENIChomozygous135851795
1242992362242992363AG50GENIChomozygous135851796