chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166999479166999480TC26GENIChomozygous108357376
1166999495166999496CT27GENIChomozygous108357377
1166999799166999800GA32GENIChomozygous109522786
1167000311167000312AG25GENIChomozygous108357378
1167004653167004654TG16GENIChomozygous109522787
1167005073167005074TC38GENIChomozygous109522788
1167005457167005458AG5GENIChomozygous108751654
1167005460167005461GT5GENIChomozygous120523139
1167005461167005462AT5GENIChomozygous120523141
1167005463167005464GA5GENIChomozygous120523143
1167007384167007385TC27GENIChomozygous108955378
1167007763167007764AC23GENIChomozygous108357389
1167007845167007846TC32GENIChomozygous108955379
1167009316167009317CT29GENIChomozygous108357390
1167009532167009533TC20GENIChomozygous108357391
1167009857167009858TC13GENIChomozygous108357392
1167010011167010012GA19GENIChomozygous108357393
1167010017167010018AG22GENIChomozygous108357394
1167011313167011314AG20GENIChomozygous108357396
1167011419167011420AG24GENIChomozygous108357397
1167011457167011458AG25GENIChomozygous108357398
1167011853167011854CT18GENIChomozygous108955386
1167011955167011956TG9GENIChomozygous108357399
1167013919167013920CT42GENIChomozygous109522789