chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225178882517889GA16GENIChomozygous115234574
1225186982518699CT16GENICpossibly homozygous115357448
1225194422519443CT10GENIChomozygous115357449
1225197682519769AG15GENIChomozygous115234576
1225200182520019AG12GENIChomozygous115357450
1225217712521772CT13GENIChomozygous115357452
1225217872521788AC14GENIChomozygous115357453
1225222782522279TC4GENIChomozygous115357454
1225222852522286TC4GENIChomozygous115357455
1225224192522421AA3GENIChomozygous132418857
1225284482528449AG25GENIChomozygous115234594
1225260842526085TC23GENIChomozygous115234584
1225267532526754TC19GENIChomozygous115234586
1225268532526854CT20GENIChomozygous115357456
1225269952526996TA17GENIChomozygous115357457
1225280722528073AT17GENIChomozygous115234588
1225284392528440CG20GENIChomozygous115234592
1225221062522110ATTT9GENIChomozygous132164545
1225224052522407AT2GENIChomozygous132164546
1225247842524801TAGAATGGAAGGGACTC13GENIChomozygous132164547
1225224142522415CA3GENIChomozygous132419480
1225297332529737ATAT12GENIChomozygous128949570
1225311672531168GA26GENIChomozygous115357458
1225317482531749AG18GENIChomozygous115234596
1225323082532309GA13GENIChomozygous115234598
1225303182530319CT11GENICheterozygous130688426
1225330652533066CG15GENIChomozygous115234600
1225334882533489CA22GENIChomozygous115234604
1225321912532192AG11GENIChomozygous115535444