chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266097358266097359GA18GENIChomozygous108637534
1266097407266097408TA24GENIChomozygous108637535
1266097625266097626GA30GENIChomozygous108637536
1266097802266097803GA42GENIChomozygous108637537
1266098310266098311AG21GENIChomozygous108637538
1266099267266099268GA53GENIChomozygous108637539
1266100423266100424AT29GENIChomozygous108637540
1266100570266100571CT46GENIChomozygous108637541
1266105178266105179CT27GENIChomozygous108637542
1266105465266105466CT44GENIChomozygous108637543
1266105615266105616TG40GENIChomozygous108637544
1266106044266106045TC53GENIChomozygous108637545
1266106110266106111AC44GENIChomozygous108637546
1266107661266107662AT35GENICpossibly homozygous108637547
1266109494266109495GC54GENICpossibly homozygous108637550
1266110219266110220AG42GENIChomozygous108637551
1266111696266111697CT42GENICheterozygous108637552
1266112073266112074AG38GENIChomozygous108637553
1266112586266112587AG46GENICpossibly homozygous108637554
1266114368266114369TG46GENIChomozygous108637555
1266114671266114672CG50GENIChomozygous108637556
1266115454266115455GA38GENICpossibly homozygous108637557
1266115499266115500GT34GENIChomozygous108637558
1266116458266116459CA37GENIChomozygous108637559
1266116647266116648CT26GENIChomozygous108637560
1266116893266116894TC29GENIChomozygous108637561
1266116961266116962CT19GENIChomozygous108637562
1266117911266117912TA38GENIChomozygous108637563
1266118863266118864TA49GENIChomozygous108637564
1266119994266119995TC53GENIChomozygous108637565
1266120026266120027TG58GENICpossibly homozygous108637566
1266120240266120241GA39GENICpossibly homozygous108637567
1266121093266121094AG33GENICpossibly homozygous108637568
1266121153266121154TC31GENICpossibly homozygous108637569
1266121498266121499TG43GENICpossibly homozygous109545657