chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1458486345848635AG11GENICpossibly homozygous804559682
1458487755848776GA17GENIChomozygous804559683
1458490205849021AG11GENIChomozygous804559684
1458491605849161AT20GENIChomozygous804559685
1458492715849272CG30GENICpossibly homozygous804559686
1458493045849305AG28GENICpossibly homozygous804559687
1458494455849446AC22GENICpossibly homozygous804559688
1458497535849754AG22GENIChomozygous804559689
1458498535849854CG22GENIChomozygous804559690
1458498725849873CT22GENIChomozygous804559691
1458498855849886AG18GENIChomozygous804559692
1458499095849910TC17GENIChomozygous804559693
1458502475850248TC21GENICpossibly homozygous804559694
1458503135850314CT14GENIChomozygous804559695
1458503145850315GT15GENIChomozygous804559696
1458506405850641CT26GENICheterozygous804559697
1458511525851153AC13GENICheterozygous804559698
1458515135851514AC7GENIChomozygous804559699
1458516555851656TC13GENICheterozygous804559700
1458517545851755CG37GENIChomozygous804559701
1458517775851778GA40GENICheterozygous804559702
1458517795851780GC40GENICheterozygous804559703
1458518305851831AG30GENICheterozygous804559704
1458526395852640TG18GENIChomozygous804559705
1458535145853515AC14GENICheterozygous804559706
1458536065853607GA27GENICheterozygous804559707
1458536995853700CT19GENICheterozygous804559708
1458537025853703AG20GENICheterozygous804559709
1458584425858443TC21GENIChomozygous804559710
1458585585858559AG21GENIChomozygous804559711
1458594115859412TC13GENIChomozygous804559712