chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104920120349201204TA19GENIChomozygous116881861
104920136249201363AG17GENIChomozygous116881863
104920173049201731CG16GENIChomozygous116881865
104920183449201835CT15GENIChomozygous116881867
104920195049201951CG11GENIChomozygous116881869
104920250349202504TC21GENIChomozygous116881871
104920317649203177CT22GENIChomozygous116881873
104920322349203224TA8GENIChomozygous116881875
104920349649203497TC10GENIChomozygous116881877
104920378649203787GA22GENIChomozygous116881879
104920448749204488TC20GENIChomozygous116881881
104920480549204806AG16GENIChomozygous116881885
104920503749205038CT18GENICheterozygous116881887
104920504049205041GA18GENIChomozygous116881889
104920590649205907GC10GENIChomozygous116881891
104920591449205915TC12GENIChomozygous116881893
104920672049206721CT15GENIChomozygous116881895
104920688249206883AT11GENIChomozygous116881897
104920715749207158AT17GENIChomozygous116881899
104920731749207318AG9GENICheterozygous117103866
104920732849207329CT6GENICheterozygous126419855
104920746249207463CT18GENIChomozygous116881901
104920749249207493CT16GENIChomozygous116881903
104920811849208119CT4GENICheterozygous118037028
104920847549208476GA6GENIChomozygous117009386
104920853349208534GA5GENIChomozygous118037033
104920883149208832GA13GENICheterozygous126382288
104920928049209281CT4GENIChomozygous116881905
104920973149209732CT10GENIChomozygous116881909