chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6125042349125042350AT50GENIChomozygous807829728
6125043149125043150GT45GENIChomozygous807829729
6125045107125045108CT56GENICpossibly homozygous807829730
6125048772125048773GA52GENIChomozygous807829731
6125049812125049813TC44GENIChomozygous807829732
6125051702125051703TC36GENICpossibly homozygous807829733
6125051787125051788GA32GENIChomozygous807829734
6125052367125052368TC27GENIChomozygous807829735
6125052674125052675CT32GENIChomozygous807829736
6125052929125052930CT51GENICpossibly homozygous807829737
6125053620125053621AG44GENIChomozygous807829738
6125054104125054105CT40GENICpossibly homozygous807829739
6125058255125058256GA27GENIChomozygous807829740
6125061110125061111GT63GENIChomozygous807829741
6125064989125064990GA36GENICpossibly homozygous807829742
6125066295125066296TC47GENIChomozygous807829743
6125067010125067011AC62GENICpossibly homozygous807829744
6125067226125067227GA39GENICheterozygous807829745
6125067234125067235AG32GENICheterozygous807829746
6125067238125067239AG40GENICheterozygous807829747
6125067989125067990CT51GENIChomozygous807829748
6125068238125068239CT42GENIChomozygous807829749
6125069020125069021TC49GENIChomozygous807829750
6125069192125069193CG24GENIChomozygous807829751
6125070462125070463GA53GENIChomozygous807829752
6125070954125070955CT52GENIChomozygous807829753
6125072010125072011GC43GENIChomozygous807829754
6125073846125073847CT52GENICpossibly homozygous807829755
6125075490125075491GA66GENIChomozygous807829756
6125077163125077164TA44GENIChomozygous807829757
6125078090125078091AG48GENIChomozygous807829758
6125081226125081227AC44GENIChomozygous807829759