chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91021659810216599GA6GENIChomozygous1000960650
91022653110226532TC9GENIChomozygous1000960651
91023446010234461AC4GENIChomozygous1000960652
91023478710234788GA6GENIChomozygous1000960653
91023561510235616GC10GENIChomozygous1000960654
91023780310237804GA2GENIChomozygous1000960655
91024115110241152CG4GENIChomozygous1000960656
91024179110241792TC2GENIChomozygous1000960657
91024266110242662AC8GENIChomozygous1000960658
91024309810243099TC3GENIChomozygous1000960659
91024411310244114GC4GENIChomozygous1000960660
91024466610244667CT12GENIChomozygous1000960661
91024486110244862AG8GENIChomozygous1000960662
91024592410245925TC4GENIChomozygous1000960663
91025022510250226AG7GENIChomozygous1000960664
91025070910250710GA3GENIChomozygous1000960665
91025071010250711GT3GENIChomozygous1000960666
91025374710253748AG10GENIChomozygous1000960667
91025494310254944CT5GENIChomozygous1000960668
91025571910255720CT9GENIChomozygous1000960669
91025859510258596GT10GENIChomozygous1000960670
91025994910259950GA5GENIChomozygous1000960671
91026048710260488CT7GENIChomozygous1000960672
91026162810261629GC2GENIChomozygous1000960673
91026490010264901AG3GENIChomozygous1000960674
91026652110266522AT5GENIChomozygous1000960675
91026850410268505GA6GENIChomozygous1000960676
91026852410268525AG6GENIChomozygous1000960677
91027097110270972CT7GENIChomozygous1000960678
91027117910271180TC7GENIChomozygous1000960679
91027947210279473TC8GENIChomozygous1000960680
91028193010281931GA4GENIChomozygous1000960681
91028198810281989GT6GENIChomozygous1000960682
91028261310282614GA6GENIChomozygous1000960683