chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174400148444001485GGAGAGAGAC18GENICheterozygous48075605
174400237444002375AG28GENIChomozygous47113500
174400252744002528A-20GENICpossibly homozygous48075606
174400330944003310AC40GENIChomozygous47113501
174400500644005007AG40GENIChomozygous47113504
174400679944006806CACACAC-------7GENICheterozygous47113507
174400681644006819CCC---12GENICheterozygous47739386
174400744744007448TC16GENIChomozygous48075607
174400775244007753TTC38GENIChomozygous47113513
174400961444009615GGAC13GENICheterozygous47998360
174401087444010875GA26GENIChomozygous48075608
174401110344011104GGGT6GENICheterozygous47113516
174401190944011910CCGATA1GENIChomozygous47856241
174401410944014110CT44GENIChomozygous48075609
174401467044014671CT47GENIChomozygous48075610
174401542544015426TC21GENIChomozygous48075611
174401878344018784GA31GENIChomozygous48075612
174401996844019969TC39GENIChomozygous47113526
174402059744020598CCACACACACACACACA41GENICheterozygous47920875
174402196044021961CCCT41GENIChomozygous48007242
174402328744023288CG44GENIChomozygous47113528
174402531244025313AG24GENIChomozygous47113531
174402569544025696TA7GENIChomozygous48007243
174401110344011104GGGTGTGT6GENICheterozygous47902998
174400681844006819C-12GENICpossibly homozygous47933625