chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706738747067388TC27GENIChomozygous997898611
104706850747068508AG24GENIChomozygous997898612
104708168047081681CT33GENIChomozygous997898613
104708237347082374GA21GENIChomozygous997898614
104708308147083082GA35GENIChomozygous997898615
104708367247083673TC29GENIChomozygous997898616
104708432247084323AG30GENIChomozygous997898617
104708446147084462TC21GENIChomozygous997898618
104708587347085874TC21GENIChomozygous997898619
104708642247086423GC25GENICpossibly homozygous997898620
104708650047086501AG43GENIChomozygous997898621
104708665247086653CA26GENIChomozygous997898622
104708734847087349GA30GENIChomozygous997898623
104708909147089092GT37GENIChomozygous997898624
104708996147089962TC16GENIChomozygous997898625
104709123347091234GA28GENIChomozygous997898626
104709128847091289GT30GENIChomozygous997898627
104709153347091534CT30GENIChomozygous997898628
104709296347092964TC20GENIChomozygous997898629
104709370847093709TC16GENIChomozygous997898630
104709387247093873GC15GENIChomozygous997898631
104709390547093906TA17GENIChomozygous997898632
104709540047095401AC16GENIChomozygous997898633
104709698847096989CT44GENIChomozygous997898634
104709700447097005TC42GENIChomozygous997898635
104709781247097813TC17GENIChomozygous997898636
104709839847098399CT25GENIChomozygous997898637
104710175847101759CT37GENIChomozygous997898638