chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106204491162044912TC25GENIChomozygous116613299
106206516662065167CT18GENIChomozygous116939563
106205956762059568GA19GENIChomozygous116939557
106206307262063073CT20GENIChomozygous116939559
106206404462064045CT18GENICpossibly homozygous116939561
106206517162065172CT15GENIChomozygous116613303
106207022562070226GA22GENIChomozygous116939565
106207241962072420GA29GENIChomozygous116939567
106207276562072766GA8GENIChomozygous116939569
106207364062073641CT38GENIChomozygous116613309
106207814362078144GA6GENIChomozygous116939571
106208162062081621GA20GENIChomozygous116939573
106208248462082485CT18GENIChomozygous116939575
106208249562082496CT18GENIChomozygous116939577
106208486662084867AG9GENIChomozygous116790897
106208549462085495TG19GENIChomozygous116613326
106208630262086303CT23GENIChomozygous116939579
106208678062086781GT15GENIChomozygous116613328
106208766162087662AG29GENIChomozygous116939581
106208767562087676CA29GENIChomozygous116613330
106208807862088079AG27GENIChomozygous116939583
106208882462088825GA21GENICpossibly homozygous116613332
106209153162091532TG11GENIChomozygous116939585
106209153462091535GT11GENIChomozygous116939587
106209153862091539TG19GENIChomozygous116939589
106208173462081735GA16GENIChomozygous117179669