chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110145666110145667TC19GENIChomozygous51601069
10110146190110146191AG17GENIChomozygous51601070
10110147331110147332GA20GENICpossibly homozygous51601073
10110147657110147658CA24GENIChomozygous51601074
10110147827110147828AC13GENICheterozygous51601075
10110148628110148629TC7GENICpossibly homozygous51601076
10110149716110149717CT18GENICheterozygous51601078
10110149768110149769TA18GENIChomozygous51601079
10110149908110149909GA31GENIChomozygous51601080
10110150002110150003GA21GENICpossibly homozygous51601081
10110150062110150063AG20GENIChomozygous51601082
10110150376110150377TA20GENICpossibly homozygous51601083
10110150488110150489AAT13GENICheterozygous51601084
10110150692110150693AG24GENIChomozygous51601085
10110150874110150875CT18GENICpossibly homozygous51601086
10110153996110153997GA9GENICpossibly homozygous51601087
10110155387110155388GA12GENIChomozygous51601093
10110156169110156170AT21GENICpossibly homozygous51601094
10110152604110152702TTTTTTTCTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAAGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCATAAG--------------------------------------------------------------------------------------------------19GENICheterozygous52410328
10110159668110159669TC24GENIChomozygous51601096
10110161214110161215CT20GENIChomozygous51601097
10110161424110161425TC20GENIChomozygous51601098
10110162074110162075AAT10GENIChomozygous51601099
10110162732110162733CT16GENICpossibly homozygous51601100
10110162960110162961GA19GENICheterozygous51601101
10110164138110164139GA20GENICpossibly homozygous51601102
10110165370110165371AG12GENIChomozygous51601103
10110165754110165755AG20GENIChomozygous51601105
10110165789110165790AG15GENICpossibly homozygous51601106
10110165895110165896TG17GENIChomozygous51601107
10110166221110166222CT8GENICpossibly homozygous51601109
10110167732110167733TC15GENICpossibly homozygous51601112
10110170818110170819TC1GENIChomozygous51601116