chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100279093100279094CT18GENIChomozygous113283820
4100280572100280573TC18GENIChomozygous113283821
4100281169100281170GT21GENIChomozygous113283822
4100284939100284940GT21GENIChomozygous113283823
4100285642100285643TC17GENIChomozygous113283824
4100288455100288456TC13GENIChomozygous113283825
4100288456100288457GA13GENIChomozygous113283826
4100288893100288894GA11GENIChomozygous113283827
4100289408100289419TTCTTTCTTTC11GENIChomozygous130935426
4100282300100282300ATCA20GENIChomozygous130935423
4100285830100285830TTAA13GENIChomozygous130935424
4100289406100289407C11GENIChomozygous130935425
4100289689100289690T9GENIChomozygous130935427
4100289714100289718ATTT7GENIChomozygous130935428
4100289748100289749AT10GENIChomozygous113283829
4100289750100289750T10GENIChomozygous130935429
4100289751100289752GA10GENIChomozygous113283830
4100289782100289783GA13GENIChomozygous113283831
4100289967100289968GA1GENIChomozygous113283832
4100290130100290131TA11GENIChomozygous113283835
4100290168100290169AT13GENICpossibly homozygous113283836
4100290660100290661AG18GENIChomozygous113283837
4100290878100290879GA13GENICpossibly homozygous113283838
4100291653100291654AG11GENIChomozygous113283839
4100291911100291913AG17GENIChomozygous130935430
4100292452100292453AT12GENIChomozygous113283840
4100292502100292503GA9GENIChomozygous113283841
4100292933100292934TC9GENIChomozygous113283842