chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104185593104185594CT26GENIChomozygous108904702
1104186011104186012AG25GENIChomozygous108904703
1104188126104188127AG18GENIChomozygous108904706
1104188215104188216AC27GENIChomozygous108904707
1104188616104188617TC23GENIChomozygous108904708
1104189183104189184GA23GENIChomozygous108904709
1104189885104189886TC9GENIChomozygous108904710
1104188319104188320GA20GENIChomozygous109119110
1104188899104188900CT18GENIChomozygous109119112
1104196180104196181TA18GENIChomozygous109119114
1104188919104188920G19GENIChomozygous130818944
1104190393104190394C24GENICpossibly homozygous130818946
1104195752104195753CA4GENIChomozygous108735625
1104195755104195761CCCCCC4GENIChomozygous127409404
1104198136104198137C1GENIChomozygous127409405
1104198173104198173C1GENIChomozygous127409406
1104198694104198695AC7GENIChomozygous108165708
1104198705104198706CA9GENIChomozygous108165709
1104198716104198718CT10GENIChomozygous127409410
1104198732104198733A14GENIChomozygous127409411
1104198849104198850G26GENIChomozygous127409412
1104199999104200000TC14GENICpossibly homozygous109119120
1104200493104200493AAATTCATCTCCAGATAAGT22GENICpossibly homozygous127409413
1104200497104200497CTGCAGAGGAAAAGGTAAACAGT13GENIChomozygous127409414
1104200500104200500TCG10GENIChomozygous127409415
1104200503104200503TGAAACAAA10GENIChomozygous127409416
1104200506104200506TGACAGATTTACCGGGGGGCATC9GENIChomozygous127409417
1104200512104200512AGATGACTAAC12GENIChomozygous127409418
1104200516104200516CTTACCCACACGTACACACGGTTTGAACAGC9GENIChomozygous127409419
1104200519104200519AACAAA12GENIChomozygous127409420
1104200763104200764TC15GENIChomozygous109119122
1104201068104201069AG20GENIChomozygous109119124
1104201244104201245GA17GENIChomozygous109119126
1104201321104201322CG17GENIChomozygous108165710
1104201340104201341CA18GENIChomozygous108165711
1104201720104201721AC16GENICpossibly homozygous108904715
1104203424104203425CT33GENIChomozygous109119128
1104200510104200511GC12GENIChomozygous127546319