chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264226142264226143CG31GENIChomozygous573149880
1264228792264228793AG23GENIChomozygous573149881
1264229240264229241CCGT15GENICheterozygous712892265
1264229240264229241CCGTGT15GENICpossibly homozygous712892266
1264229310264229311TC21GENIChomozygous573149882
1264230653264230654GGT8GENICpossibly homozygous712892269
1264230657264230658GT19GENIChomozygous573149883
1264231202264231203GGTGGTT15GENIChomozygous712892271
1264231476264231477A-1GENIChomozygous712892272
1264231777264231813AAGAAAGGAAGAAAGGAAGAAAGAAAGAAAGAAAGA------------------------------------17GENIChomozygous712892273
1264232052264232053TC13GENIChomozygous573149884
1264233092264233093GA22GENIChomozygous573149885
1264234032264234036ATTT----1GENIChomozygous712892276
1264235077264235078GA22GENIChomozygous573149886
1264235389264235390G-26GENIChomozygous712892277
1264235500264235501T-5GENICheterozygous712892279
1264235937264235938T-6GENIChomozygous712892282
1264236612264236613AG29GENIChomozygous573149887
1264236684264236685CG23GENIChomozygous575239078
1264237128264237129GT29GENIChomozygous573149888
1264237824264237825GC41GENIChomozygous573149889
1264237845264237846GA46GENIChomozygous573149890
1264237893264237894CT49GENIChomozygous573149891
1264238519264238520TC32GENIChomozygous573149892
1264239237264239238AG20GENIChomozygous573149893
1264239837264239838GA12GENIChomozygous573149894
1264240685264240686CT25GENIChomozygous573149895
1264240881264240882AG12GENIChomozygous573149896
1264240961264240962AG14GENIChomozygous573149897
1264241000264241001AG14GENIChomozygous573149898
1264241159264241160GA17GENIChomozygous573149899
1264241332264241333AG19GENIChomozygous573149900