chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85811553758115538TC9GENICpossibly homozygous52982030
85811555158115555ACTT----10GENIChomozygous53121709
85811558658115587T-12GENIChomozygous52982031
85811559558115596TTC15GENIChomozygous52658330
85811565158115652AC15GENIChomozygous52982032
85811619758116198AC13GENIChomozygous52658334
85811653458116535GT27GENIChomozygous52982034
85811719258117193GA20GENIChomozygous52982036
85811764758117648AC20GENIChomozygous53121711
85811768358117684GA16GENIChomozygous52982038
85811771158117712AG16GENIChomozygous52982039
85811772658117727AG17GENIChomozygous52658338
85811815058118151TC34GENIChomozygous52982040
85811923558119236AATGTTGTTGT18GENIChomozygous52982046
85811923858119239AT20GENIChomozygous52982047
85811937058119371TC26GENIChomozygous52658340
85811956758119568TC26GENIChomozygous52982050
85811990358119904CT23GENIChomozygous52658344
85812026458120265TTCTC29GENIChomozygous52982051
85812067558120676CT23GENIChomozygous53121712
85812071558120716GC22GENIChomozygous52982053
85812101058121011AG20GENIChomozygous52982054
85812140558121406AG9GENIChomozygous52982055