chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102885705028857051TC57GENIChomozygous51384153
102885720728857208TTGC42GENIChomozygous51384154
102885923228859233AG40GENIChomozygous51384155
102886106528861066AG48GENIChomozygous51384156
102886222428862225CT13GENIChomozygous51384157
102886224428862245GT10GENICpossibly homozygous51384158
102886354128863542GGT28GENIChomozygous51384159
102886383628863837GA70GENIChomozygous51384160
102886420028864201CA53GENIChomozygous51384161
102886420528864206GA56GENIChomozygous51384162
102886423028864231AC39GENIChomozygous51384163
102886435928864360AATG20GENICheterozygous51384164
102886436028864368CGCGCACG--------20GENICheterozygous51384165
102886436728864368GA24GENICpossibly homozygous51384166
102886437128864372GA21GENICpossibly homozygous51384167
102886437328864374GA19GENICpossibly homozygous51384168
102886437928864380GA17GENIChomozygous51384169
102886570928865710AG26GENIChomozygous51384170
102886579928865800CA42GENIChomozygous51384171
102886583628865837CT30GENICpossibly homozygous51384172
102886589928865900CT42GENIChomozygous51384173
102886590128865902GA44GENIChomozygous51384174
102886590328865904CT46GENIChomozygous51384175
102886595028865951GT41GENIChomozygous51384176
102886595628865957GC35GENIChomozygous51384177
102886601328866014GA38GENIChomozygous51384178
102886602428866025C-33GENIChomozygous51384179
102886602628866027CCAG33GENIChomozygous51384180
102886610828866109CT39GENICpossibly homozygous51384181
102886619128866192T-37GENIChomozygous51384182
102886624928866250T-37GENIChomozygous51384183
102886648728866488GGA53GENIChomozygous51384184
102886680028866801GA58GENIChomozygous51384185
102886707128867072CG43GENIChomozygous51384186
102886708928867090TTG34GENIChomozygous51384187
102886744928867450AG55GENIChomozygous51384188
102886780728867808CG29GENIChomozygous51384189