chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46490156264901562A60GENIChomozygous128042750
46491856164918562C47GENIChomozygous128042759
46491856864918569G46GENIChomozygous128042760
46491862664918627C34GENIChomozygous128042761
46491862864918629CG34GENIChomozygous119277400
46491863264918633G32GENIChomozygous128042762
46491863964918640C32GENIChomozygous128042763
46491864664918648AT31GENIChomozygous128042764
46492242264922424AT37GENIChomozygous128042765
46492242664922427G39GENIChomozygous128042766
46492243964922440T40GENIChomozygous128042767
46492244664922447G42GENIChomozygous128042768
46492245264922453AT41GENIChomozygous112681209
46492253064922530G36GENIChomozygous128042769
46492253564922536C35GENIChomozygous128042770
46492254864922549TC33GENIChomozygous112681211
46492261064922611C20GENIChomozygous128042771
46492262264922623CA18GENIChomozygous112681213
46492881764928817AAAGAAGTGCCACCACGATCTTCTGCTCACCTCTTTCTAACAGTTTTCTGCCCCAGCAGCCCATTCAGAAGGAAACAGGAAAGACAAACCCCCAGTTCATTGAACTGTACACAGAGTCTGTGTGTGGAACCAATGAGCTGCTGGACCACCCCGCCACCTTG44GENICpossibly homozygous128042774
46492268164922683CA9GENIChomozygous128042772
46492269664922697C8GENIChomozygous128042773