chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3157675316157675317TC4GENICheterozygous125896407
3157708441157708442AG10GENIChomozygous111788902
3157767319157767320GA20GENIChomozygous111788916
3157769629157769630AT3GENICheterozygous125985574
3157791469157791470TC6GENICheterozygous125985576
3157805266157805267GT5GENIChomozygous125852351
3157823276157823277TC17GENIChomozygous125840681
3157899107157899108TC22GENIChomozygous111788948
3157921986157921987TC8GENIChomozygous125840682
3157938516157938517TC12GENIChomozygous125840683
3157938539157938540GT6GENIChomozygous125840684
3157938550157938551CA6GENIChomozygous125852352
3158013630158013631TC5GENICheterozygous125840685
3158017321158017322AC6GENIChomozygous111788962
3158017322158017323AG6GENIChomozygous111788964
3158130514158130515CT7GENIChomozygous125840686
3158130575158130576TG16GENIChomozygous125840687
3158134096158134097GA18GENIChomozygous111788968
3158134177158134178CT10GENIChomozygous111788970
3158134211158134212TC9GENIChomozygous111788972
3158134214158134215CG8GENIChomozygous111788974
3158136145158136146TA6GENICheterozygous125985578
3158209727158209728CG4GENIChomozygous125896522
3158209775158209776CT8GENIChomozygous125840688
3158209805158209806CT6GENIChomozygous125840689
3158209814158209815GT6GENIChomozygous125840690
3158209827158209828CT8GENIChomozygous125840691
3158209857158209858CT13GENIChomozygous125840692
3158253905158253906AC18GENIChomozygous111788980