chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104185593104185594CT51GENIChomozygous108904702
1104186011104186012AG60GENICpossibly homozygous108904703
1104188126104188127AG38GENIChomozygous108904706
1104188215104188216AC47GENIChomozygous108904707
1104188319104188320GA47GENIChomozygous109119110
1104188616104188617TC36GENIChomozygous108904708
1104188899104188900CT51GENIChomozygous109119112
1104189183104189184GA56GENICpossibly homozygous108904709
1104189885104189886TC51GENIChomozygous108904710
1104195752104195753CA5GENIChomozygous108735625
1104196180104196181TA65GENICpossibly homozygous109119114
1104198018104198019AC42GENICpossibly homozygous108165703
1104198438104198439CA31GENICpossibly homozygous108165705
1104198586104198587GA42GENICheterozygous109119116
1104198621104198622CT183GENICheterozygous109119118
1104198624104198625TA192GENIChomozygous108165706
1104198629104198630CT219GENICheterozygous108165707
1104198694104198695AC190GENICheterozygous108165708
1104198705104198706CA121GENIChomozygous108165709
1104198894104198895AC32GENICheterozygous109509400
1104199999104200000TC51GENIChomozygous109119120
1104200763104200764TC40GENIChomozygous109119122
1104201068104201069AG50GENIChomozygous109119124
1104201244104201245GA48GENIChomozygous109119126
1104201321104201322CG42GENIChomozygous108165710
1104201340104201341CA39GENIChomozygous108165711
1104201720104201721AC53GENIChomozygous108904715
1104203424104203425CT36GENIChomozygous109119128