chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104597884245978843CCGT19GENIChomozygous52496902
104597884345978844CG19GENIChomozygous52496905
104597884545978846GGTGT18GENIChomozygous52459296
104597884845978859CCCCCCCCACC-----------19GENIChomozygous52373288
104597886045978861AT13GENIChomozygous52373290
104597886245978882ATAAAAAGATAAATAGAAAC--------------------25GENIChomozygous52373292
104597888345978884AG19GENIChomozygous52373294
104597888545978886TG16GENIChomozygous52373296
104597888845978889TTGC16GENIChomozygous52373298
104597889145978894TTT---18GENIChomozygous52373300
104597889545978896TC17GENIChomozygous52373302
104597889745978908TAAATTTTATT-----------19GENIChomozygous52373304
104597891045978911T-19GENIChomozygous52373306
104597891245978913AAC19GENIChomozygous52373308
104599150645991507AG32GENIChomozygous51443658
104599289245992897GGGGC-----17GENICheterozygous52373310
104599289245992896GGGG----17GENICpossibly homozygous52373312
104599289545992896GGAAAA16GENICpossibly homozygous52373314
104599441845994419A-19GENIChomozygous51636592
104599583245995833GGT32GENIChomozygous51443674