chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264226142264226143CG6GENIChomozygous646060895
1264226521264226522A-10GENIChomozygous754740512
1264226915264226916TA35GENIChomozygous646060896
1264227340264227341AG25GENIChomozygous646060897
1264227404264227405GA19GENIChomozygous646060898
1264228792264228793AG20GENIChomozygous646060899
1264229240264229241CCGTGTGTGT2GENIChomozygous754740515
1264229310264229311TC9GENIChomozygous646060900
1264230653264230654GGT16GENICheterozygous754740517
1264230653264230654GGTTT16GENICpossibly homozygous754740518
1264230657264230658GT21GENIChomozygous646060901
1264231202264231203GGTGGTT16GENIChomozygous754740519
1264231476264231477A-10GENIChomozygous754740520
1264231777264231813AAGAAAGGAAGAAAGGAAGAAAGAAAGAAAGAAAGA------------------------------------22GENIChomozygous754740521
1264232052264232053TC27GENIChomozygous646060902
1264233092264233093GA33GENIChomozygous646060903
1264235077264235078GA26GENIChomozygous646060904
1264235389264235390G-25GENICpossibly homozygous754740523
1264235498264235499AAT11GENIChomozygous754740526
1264235937264235938T-14GENICpossibly homozygous754740528
1264236612264236613AG24GENIChomozygous646060905
1264237128264237129GT23GENIChomozygous646060906
1264237824264237825GC26GENIChomozygous646060907
1264237845264237846GA25GENIChomozygous646060908
1264237893264237894CT15GENIChomozygous646060909
1264237905264237906GA15GENIChomozygous646060910
1264237932264237933CA17GENIChomozygous646060911
1264238519264238520TC19GENIChomozygous646060912
1264239237264239238AG14GENIChomozygous646060913
1264239746264239747CCT6GENIChomozygous754740529
1264239837264239838GA10GENIChomozygous646060914
1264240127264240130TTT---5GENIChomozygous754740530
1264240661264240665AATC----29GENIChomozygous754740531
1264240881264240882AG30GENIChomozygous646060915
1264240961264240962AG31GENIChomozygous646060916
1264241000264241001AG37GENIChomozygous646060917