chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113541563635415637A-16GENICheterozygous50924639
113541563735415638C-12GENIChomozygous50924641
113541658435416585T-14GENICpossibly homozygous50729324
113541679135416792T-15GENIChomozygous50924645
113541740735417408T-21GENIChomozygous50729325
113541784635417847AAT13GENIChomozygous50729326
113542071035420711TTG14GENIChomozygous50924648
113542081935420820TG20GENIChomozygous50729331
113542183235421833CT31GENIChomozygous50924651
113542534035425341CT26GENICpossibly homozygous50729334
113542536335425364TC21GENIChomozygous50729335
113542773135427732TTC20GENIChomozygous50924654
113542793535427936GA18GENIChomozygous50924657
113542858535428586CG26GENIChomozygous50729339
113543330535433306AG32GENIChomozygous50924660
113543444735434448AC36GENIChomozygous50924663
113543484035434841TC23GENIChomozygous50729343
113543571235435713GA25GENIChomozygous50924666
113543581935435820TC29GENIChomozygous50729348
113543613835436139T-29GENIChomozygous50924669
113543711235437113A-29GENIChomozygous50729351
113543801835438019AC24GENIChomozygous50924672
113544233635442337TC19GENIChomozygous50729357
113544292135442922TC20GENIChomozygous50729359
113544371935443721AG--25GENIChomozygous50729362
113544377935443780AAG23GENIChomozygous50924675
113544378235443783AC25GENIChomozygous50924678
113544444235444443TC23GENIChomozygous50729363
113544516235445163TC29GENIChomozygous50924681
113544517435445175GA26GENIChomozygous50729366