chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147646480147646481TC22GENIChomozygous112874690
4147647140147647141GC23GENICheterozygous112874692
4147647144147647145GC22GENICpossibly homozygous112874693
4147647276147647277GC20GENIChomozygous112874694
4147647675147647676TC20GENIChomozygous113180273
4147647679147647680TC19GENICheterozygous113180274
4147647683147647684TC18GENICheterozygous113180275
4147647687147647688TC18GENICheterozygous113180276
4147647953147647954TG24GENIChomozygous112874696
4147648041147648042AG14GENIChomozygous112874697
4147648845147648846TG19GENIChomozygous112874698
4147648853147648854GA21GENIChomozygous112874699
4147649168147649169TC23GENIChomozygous112874700
4147649567147649568CG27GENIChomozygous112874701
4147650839147650840TC19GENIChomozygous112874702
4147650843147650844TC19GENIChomozygous112874703
4147651493147651494AG23GENIChomozygous112874704
4147651859147651860CA21GENIChomozygous112874706
4147652015147652016CT14GENIChomozygous112874707
4147652756147652757AG33GENIChomozygous112874708
4147653087147653088TC16GENIChomozygous112874709
4147653534147653535TA15GENIChomozygous112874710
4147653566147653567CT15GENIChomozygous112874711
4147654275147654276CT13GENIChomozygous112874712
4147655298147655299CT15GENIChomozygous112874713
4147655719147655720AT6GENICheterozygous112874714
4147655883147655884TA54GENICheterozygous113059336
4147655888147655889TA58GENICheterozygous113059338
4147655978147655979AT44GENICheterozygous112874721
4147655988147655989TA41GENICheterozygous113180277
4147655993147655994TA40GENICheterozygous113180278
4147656072147656073TA30GENICheterozygous112874723
4147656097147656098TA32GENICheterozygous112874724
4147656162147656163AT43GENICheterozygous113180279
4147656182147656183AT31GENICheterozygous113059348
4147656242147656243AT22GENICheterozygous112874725