chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204409222844092229GA55GENIChomozygous142738656
204409224744092248TC56GENIChomozygous130114527
204409226644092267TC61GENIChomozygous130114530
204409638044096381AG61GENIChomozygous142738657
204409654744096548CA45GENIChomozygous142738658
204409689444096895CA61GENICpossibly homozygous142738659
204409712144097122TC51GENICpossibly homozygous142738660
204409754644097547CT46GENIChomozygous142738661
204409754644097547C46GENICheterozygous403470827
204409755144097552CA47GENIChomozygous142738662
204409831644098317CT16GENIChomozygous142738663
204410124044101241AG56GENIChomozygous130114583
204410158744101588CG36GENIChomozygous142738664
204410275844102759TC55GENIChomozygous142738665
204410295544102956AG71GENIChomozygous142738666
204410318444103185CT60GENIChomozygous142738667
204410322544103226TC61GENIChomozygous130114593
204410336844103369TG65GENIChomozygous142738668
204410350944103510CT68GENIChomozygous142738669
204410375544103756AG58GENIChomozygous130114599
204410601844106019TC53GENIChomozygous130114606
204410663644106637AG58GENIChomozygous142738670
204410705844107059AT47GENIChomozygous142738671
204410706844107069CT49GENIChomozygous142738672
204410735244107353CA41GENIChomozygous142738673
204410747844107479TA56GENIChomozygous142738674
204410823544108236AG50GENIChomozygous142738675
204410896244108963A25GENICpossibly homozygous403470828
204410896244108963AC25GENICheterozygous403470829
204410908444109085TG25GENIChomozygous142738676
204409960044099613TCTCTCTCTCTCT6GENICheterozygous145086401
204409966044099660CAAGTTTAGTTACTGAACCATACTGAAG17GENIChomozygous130000657
204409829144098291TC16GENIChomozygous142715528
204409829744098297TCTCTT16GENIChomozygous142715529
204410329844103299A53GENIChomozygous142715530
204410908144109081A24GENIChomozygous142715531
204409959844099599T6GENICheterozygous145086400