chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109794098397940984C10GENIChomozygous128850840
109794098997940990A11GENIChomozygous128850841
109794099397940994C12GENIChomozygous128850842
109794099497940995CT12GENIChomozygous116907048
109794099897940999C12GENIChomozygous128850843
109794100297941003A12GENIChomozygous128850844
109794100497941006CT12GENIChomozygous128850845
109794107797941077C12GENIChomozygous128850846
109794116097941160C7GENIChomozygous128850847
109794119797941197C6GENIChomozygous128850848
109794122697941227C5GENIChomozygous128850849
109794123197941232C5GENIChomozygous128850850
109794125597941256C6GENIChomozygous128850851
109794131197941311CGCC7GENIChomozygous128850852
109794131797941318A7GENIChomozygous128850853
109794141897941419C8GENIChomozygous128850854
109794143897941438G9GENIChomozygous128850855
109794144497941444CC8GENIChomozygous128850856
109794146097941461C7GENIChomozygous128850857
109794675697946757CT14GENIChomozygous116695402
109794164297941643TC13GENIChomozygous116695392
109794232697942327CT12GENIChomozygous116695394
109794289897942899CT17GENIChomozygous116695396
109794438897944389AT22GENIChomozygous116695398
109794485297944853AG20GENIChomozygous116695400
109794704197947042CT13GENIChomozygous116695404
109794716697947167GT3GENIChomozygous129974028
109794716897947169AC3GENIChomozygous129974029
109794768597947686AG13GENIChomozygous116695406
109794813397948151TCCTTCCCTTCCTTCCCT13GENIChomozygous128850859
109794909697949097TG11GENIChomozygous116695408
109795035597950356CA13GENIChomozygous116695410
109795141297951413AG11GENIChomozygous116695412
109795166297951663AC16GENIChomozygous116695414
109795577197955772CG20GENIChomozygous116695424
109795281497952815TC16GENIChomozygous116695416
109795389197953892GT13GENIChomozygous116695418
109795413197954132CG11GENIChomozygous116695420
109795525197955252TC18GENIChomozygous116695422
109795380297953803CT12GENIChomozygous118010454
109795794297957944TG13GENIChomozygous128850860
109795885297958853GC14GENIChomozygous116695426