chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2138592048138592049GA20GENIChomozygous60976642
2138593080138593081TC30GENIChomozygous59862114
2138595582138595583CCGT10GENICheterozygous60976644
2138595637138595641GTCT----14GENIChomozygous60976646
2138595958138595959TTAA10GENICheterozygous59862145
2138595958138595959TTA10GENICheterozygous60976648
2138597156138597164CACACACA--------9GENICheterozygous60499443
2138597162138597164CA--9GENICpossibly homozygous60754497
2138600384138600385T-7GENICpossibly homozygous60976650
2138600409138600410GGTGTATGTA13GENIChomozygous60976652
2138605095138605096CCGT1GENIChomozygous60976654
2138605531138605532TTGGTTTTTTTTTTTTTTTGGTTCTTTTTTCCGG2GENIChomozygous60754499
2138605533138605534CG2GENIChomozygous60754501
2138606487138606488AG15GENIChomozygous59114702
2138611292138611293TC22GENIChomozygous60976656
2138612765138612767AC--11GENICheterozygous60976658
2138612878138612879GA24GENIChomozygous60976660
2138613969138613970CCT17GENIChomozygous60499449
2138615937138615939TT--14GENICpossibly homozygous59862245
2138616063138616064GT17GENIChomozygous60976662
2138617297138617298A-25GENICpossibly homozygous60976664
2138618034138618035TTGGCCACTATTA22GENIChomozygous59862263
2138618475138618476TTACAC7GENIChomozygous60891342
2138620791138620792CCTT5GENICheterozygous60499450
2138623311138623312GA12GENIChomozygous60976666
2138625993138625994GGT21GENIChomozygous59114706
2138626168138626170GA--21GENIChomozygous60976668
2138626755138626760CACAG-----3GENIChomozygous60976670