chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3145653094145653095CT44GENIChomozygous148471283
3145653136145653137CT48GENIChomozygous148471284
3145653842145653843CA53GENIChomozygous149024328
3145654584145654585CA49GENIChomozygous143031843
3145655234145655235T40GENIChomozygous148460103
3145656202145656203AG46GENIChomozygous143031844
3145656619145656620CT36GENIChomozygous148869138
3145656747145656748CG42GENIChomozygous143031845
3145656748145656749CT42GENIChomozygous143031846
3145656833145656834TC42GENIChomozygous143031847
3145656902145656903AG40GENIChomozygous143031848
3145657348145657349CA43GENIChomozygous143031849
3145657767145657768GA46GENICpossibly homozygous143031850
3145657964145657965AG51GENIChomozygous143031851
3145658650145658651AC52GENIChomozygous143031856
3145658817145658818AC51GENIChomozygous143031857
3145659325145659326CT45GENIChomozygous149024329
3145661401145661402AT57GENIChomozygous149024330
3145661629145661630CA49GENIChomozygous143031859
3145661998145661999CT43GENIChomozygous143031860
3145662305145662306AG53GENIChomozygous143031861
3145662695145662696AG41GENIChomozygous143031862
3145663028145663029TC41GENIChomozygous149024331
3145664733145664734CT48GENICpossibly homozygous148869141
3145657262145657263GC44GENIChomozygous145431228
3145663980145663981GA45GENIChomozygous148869140
3145660154145660155G45GENIChomozygous149022429
3145661147145661147C30GENIChomozygous149022430
3145666037145666038TC55GENIChomozygous143031866
3145667305145667306CT36GENIChomozygous143031867
3145667647145667648TC58GENIChomozygous143031868