chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
995794729579473CT8GENIChomozygous619007113
995854589585459TTC2GENICheterozygous742726740
995881049588105CT12GENIChomozygous619007114
995884589588459AC13GENIChomozygous619007115
995891849589185G-8GENIChomozygous742726741
995942079594208GGT13GENIChomozygous742726742
996008339600834C-8GENIChomozygous742726743
996036099603610TC18GENIChomozygous619007116
996076249607625GGA8GENICheterozygous742726745
996135579613558TTC6GENICheterozygous742726746
996135579613558TTCCC6GENICheterozygous742726747
996149809614982TT--10GENIChomozygous742726748
996150059615006CT13GENIChomozygous619007117
996153869615387AT18GENIChomozygous619007118
996195799619580CCCA16GENIChomozygous742726750
996195829619583G-16GENIChomozygous742726751
996195849619585TTCA15GENIChomozygous742726752
996195859619586GC16GENIChomozygous619007119
996205209620521AG20GENIChomozygous619007120
996251939625194TG16GENIChomozygous619007121
996252029625203CCT19GENIChomozygous742726753
996252389625243TTTTT-----11GENICpossibly homozygous742726754
996252429625243T-11GENICheterozygous742726756
996268099626810AC1GENIChomozygous619007122
996307999630800TTCACACACA2GENIChomozygous742726759
996327209632721AG4GENIChomozygous619007123
996340709634071C-3GENICheterozygous742726761
996340729634085CACACACACACAC-------------3GENICheterozygous742726762
996372449637245CA9GENIChomozygous619007124