chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143310913433109135CT8GENIChomozygous113417757
143311007733110078AG21GENIChomozygous113417758
143311042733110428AG21GENIChomozygous113417759
143311209233112093AC16GENIChomozygous113417760
143311215933112160CA23GENIChomozygous113417761
143311313333113134TA24GENIChomozygous113417762
143311405433114055CA8GENIChomozygous113417763
143311431333114314GT10GENICheterozygous113417764
143311435133114352TC18GENIChomozygous113417765
143311490633114907TC19GENIChomozygous113417766
143311548433115485AG17GENIChomozygous113417767
143311659233116593AC9GENIChomozygous113672234
143311739233117393GA7GENIChomozygous113417768
143312054533120546TC15GENIChomozygous113417769
143312278533122786AG7GENIChomozygous113672236
143312282633122827TC7GENIChomozygous113417771
143312283833122839TC6GENIChomozygous113417772
143312300433123005CT10GENIChomozygous113584880
143312303333123034AG6GENIChomozygous113786900
143312342033123421TC14GENIChomozygous113417773
143312370633123707TC28GENIChomozygous113417774
143312377533123776GA20GENIChomozygous113417775
143312383333123834GA13GENIChomozygous113417776
143312397733123978AG16GENIChomozygous113417777
143312404533124046GA15GENIChomozygous113417778