chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18601713086017131A10GENICheterozygous402951690
18601713086017131AT10GENICheterozygous402951691
18601713286017133A11GENICheterozygous402951692
18601713286017133AT11GENICheterozygous402951693
18601713486017135A9GENICheterozygous402951694
18601713486017135AT9GENICheterozygous402951695
18601727386017274GA44GENIChomozygous142842989
18601732486017325AG40GENIChomozygous142842990
18601808086018081TC23GENIChomozygous142842991
18601830086018301T30GENIChomozygous402951696
18601830086018301TC30GENICheterozygous402951697
18601979886019799CT52GENIChomozygous142842992
18602004786020048GA55GENIChomozygous142842993
18602380886023861CACTGAGCCACGCCCCCAGCCCCTCACTGGGGGATTCTAGGCAGGGGCTCTAT38GENICpossibly homozygous142790346
18602026186020267CAGAAG50GENIChomozygous142790345
18602128786021288GA40GENIChomozygous142842994
18602278986022790AG47GENIChomozygous142842995
18602284486022845AG44GENIChomozygous142842996
18602291386022914AG40GENIChomozygous142842997
18602371286023713TA29GENIChomozygous142842998
18602440386024404CT12GENIChomozygous142842999
18602480386024804TC18GENIChomozygous142843000
18602578686025787GA48GENIChomozygous142843001
18602595886025959TC65GENIChomozygous142843002
18602641986026420TG51GENIChomozygous142843003
18602695686026958TA34GENIChomozygous142790347
18602784086027841GA65GENIChomozygous142843004
18602799286027993TA42GENIChomozygous142843005
18602907986029080CT48GENICpossibly homozygous142843006
18602934286029343GA52GENIChomozygous142843007
18603028286030283GC39GENIChomozygous142843008
18603109286031093AG40GENIChomozygous142843009
18602645386026455GA35GENICheterozygous144228721