chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5114943314114943315GA11GENIChomozygous119177148
5114943679114943680AG13GENIChomozygous113971431
5114949643114949644CT13GENIChomozygous113971436
5114959631114959632CT20GENIChomozygous119203890
5114960447114960448TA17GENIChomozygous113971457
5114960496114960497GA15GENIChomozygous119177150
5114961709114961710AC4GENICheterozygous126201892
5114962275114962276AG4GENIChomozygous113971462
5114963529114963530CA20GENIChomozygous119203891
5114964050114964051TC9GENIChomozygous113971467
5114970096114970097GA15GENIChomozygous119177152
5114975165114975166AT8GENICheterozygous126311214
5114975939114975940CG6GENICheterozygous126278475
5114978662114978663CT16GENIChomozygous119177154
5114978833114978834AG12GENIChomozygous113971483
5114984423114984424TG19GENIChomozygous119177156
5114988159114988160CT11GENIChomozygous119177158
5114998721114998722TC17GENIChomozygous119177162