chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47802613078026131GA18GENIChomozygous113124764
47802752178027522GA30GENIChomozygous119307339
47802784578027846AG30GENIChomozygous112737446
47802848878028489GC22GENIChomozygous112737448
47802850278028503CG20GENIChomozygous113124765
47802975478029755TG30GENIChomozygous112737450
47803003878030039CT23GENIChomozygous113124766
47803073678030737GA27GENIChomozygous113124767
47803174478031745AG28GENIChomozygous112737454
47803187178031872TC31GENIChomozygous112737458
47803218678032187CT13GENIChomozygous113124768
47803405378034054AG15GENIChomozygous112737460
47803409278034093TC16GENIChomozygous112737462
47803517678035177GT19GENIChomozygous113124769
47803599778035998AG21GENIChomozygous112737466
47803684978036850TA30GENIChomozygous112737470
47803711878037119GA27GENIChomozygous113124770
47803789378037894GA26GENIChomozygous113124771
47804006178040062GA17GENIChomozygous112737474
47804037378040374AT20GENIChomozygous112737476
47804070578040706GA27GENIChomozygous113124772
47804072978040730TC26GENIChomozygous112737478
47804161978041620TC25GENIChomozygous112737480
47804191478041915GA17GENIChomozygous112737482
47804229178042292CG20GENIChomozygous112737484
47804378478043785GA16GENIChomozygous112737486
47804401178044012AG16GENIChomozygous112737488
47804592878045929CG21GENIChomozygous112737492
47804627278046273GA26GENIChomozygous112737494