chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204409222844092229GA19GENIChomozygous142738656
204409224744092248TC18GENIChomozygous130114527
204409226644092267TC18GENIChomozygous130114530
204409638044096381AG20GENIChomozygous142738657
204409654744096548CA13GENIChomozygous142738658
204409689444096895CA13GENIChomozygous142738659
204409712144097122TC12GENIChomozygous142738660
204409754644097547CT12GENIChomozygous142738661
204409755144097552CA13GENIChomozygous142738662
204409831644098317CT5GENIChomozygous142738663
204410124044101241AG28GENIChomozygous130114583
204410158744101588CG18GENICpossibly homozygous142738664
204410275844102759TC16GENIChomozygous142738665
204410295544102956AG19GENIChomozygous142738666
204410318444103185CT14GENIChomozygous142738667
204410322544103226TC14GENIChomozygous130114593
204409829144098291TC5GENIChomozygous142715528
204409966044099660CAAGTTTAGTTACTGAACCATACTGAAG13GENIChomozygous130000657
204409829744098297TCTCTT5GENIChomozygous142715529
204410329844103299A15GENIChomozygous142715530
204409959844099599T6GENIChomozygous145086400
204409960044099613TCTCTCTCTCTCT6GENIChomozygous145086401
204410336844103369TG20GENIChomozygous142738668
204410350944103510CT22GENIChomozygous142738669
204410375544103756AG18GENIChomozygous130114599
204410601844106019TC32GENIChomozygous130114606
204410663644106637AG15GENIChomozygous142738670
204410705844107059AT22GENIChomozygous142738671
204410706844107069CT18GENIChomozygous142738672
204410735244107353CA23GENIChomozygous142738673
204410747844107479TA20GENIChomozygous142738674
204410823544108236AG11GENIChomozygous142738675
204410908444109085TG9GENIChomozygous142738676
204410908144109081A11GENIChomozygous142715531