chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143310913433109135CT12GENIChomozygous113417757
143311007733110078AG29GENIChomozygous113417758
143311042733110428AG32GENIChomozygous113417759
143311209233112093AC25GENIChomozygous113417760
143311215933112160CA30GENIChomozygous113417761
143311313333113134TA27GENIChomozygous113417762
143311405433114055CA11GENIChomozygous113417763
143311419733114198TC6GENIChomozygous113978541
143311431333114314GT21GENIChomozygous113417764
143311435133114352TC19GENIChomozygous113417765
143311490633114907TC32GENIChomozygous113417766
143311548433115485AG19GENIChomozygous113417767
143311659233116593AC12GENIChomozygous113672234
143311739233117393GA18GENIChomozygous113417768
143312054533120546TC19GENIChomozygous113417769
143312069033120691AG18GENIChomozygous113417770
143312278533122786AG19GENIChomozygous113672236
143312282633122827TC14GENIChomozygous113417771
143312283833122839TC15GENIChomozygous113417772
143312370633123707TC32GENIChomozygous113417774
143312377533123776GA30GENIChomozygous113417775
143312383333123834GA30GENIChomozygous113417776
143312397733123978AG29GENIChomozygous113417777
143312404533124046GA26GENIChomozygous113417778
143312300433123005CT25GENICpossibly homozygous113584880