chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102885720728857208TTGC30GENIChomozygous51384154
102885840628858407GA37GENIChomozygous52036850
102885881528858816CCT6GENICheterozygous51633486
102885883528858839ATTT----6GENIChomozygous52036852
102885900528859018CCCCAGTTCTCAA-------------10GENIChomozygous52036854
102885923228859233AG14GENIChomozygous51384155
102886006828860069GA16GENIChomozygous52036856
102886106528861066AG33GENIChomozygous51384156
102886212328862124GA10GENIChomozygous52036858
102886222428862225CT3GENIChomozygous51384157
102886223228862233G-2GENIChomozygous52036860
102886357528863576TC14GENIChomozygous52036862
102886383628863837GA21GENIChomozygous51384160
102886420028864201CA22GENIChomozygous51384161
102886420528864206GA22GENIChomozygous51384162
102886423028864231AC19GENIChomozygous51384163
102886436028864368CGCGCACG--------17GENIChomozygous51384165
102886560028865601GA19GENIChomozygous52036866
102886570928865710AG27GENIChomozygous51384170
102886583628865837CT21GENIChomozygous51384172
102886589928865900CT25GENIChomozygous51384173
102886590328865904CT24GENIChomozygous51384175
102886593028865931GGGGC27GENIChomozygous52036868
102886593128865932AAACTG28GENIChomozygous52036870
102886602428866025C-20GENIChomozygous51384179
102886602628866027CCAG22GENIChomozygous51384180
102886610828866109CT17GENIChomozygous51384181
102886624928866250T-13GENIChomozygous51384183
102886632828866329TC14GENIChomozygous52036872
102886648728866488GGA13GENIChomozygous51384184
102886657228866573CA26GENIChomozygous52036874
102886680028866801GA16GENIChomozygous51384185
102886707128867072CG18GENIChomozygous51384186
102886712828867129TG18GENIChomozygous52036876
102886436828864369CT16GENIChomozygous52363490
102886438028864444CACACGCACGCGCACACGCACGCGCACACACACGCGCACACACACACACACACACACACACACA----------------------------------------------------------------30GENIChomozygous52315261
102886537328865387AAAAAAAAAAAAAA--------------5GENICheterozygous52458291