chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102941599102941600TC16GENIChomozygous109115427
1102944242102944243AG21GENIChomozygous109115429
1102945598102945599CT19GENIChomozygous109115433
1102946046102946047AG20GENIChomozygous120503647
1102946047102946048TA20GENIChomozygous120503648
1102947136102947137TA19GENIChomozygous109115435
1102947607102947608TC21GENIChomozygous109115437
1102947653102947654TA20GENIChomozygous109115439
1102947528102947528C19GENIChomozygous130818477
1102947579102947579C21GENIChomozygous130818478
1102948656102948656A10GENIChomozygous130818479
1102950349102950350CT18GENIChomozygous109115441
1102953494102953495CT25GENIChomozygous109115443
1102954626102954627CT15GENIChomozygous109115447
1102957497102957498TC22GENIChomozygous109115449
1102958021102958022AT25GENIChomozygous109115451
1102958165102958166CT18GENIChomozygous109115453
1102958201102958202AG19GENIChomozygous109115455
1102960758102960759AG18GENIChomozygous109115457
1102965291102965292TC18GENIChomozygous109115459
1102968260102968261TA20GENIChomozygous109115461
1102969965102969965AGGAGGAGG17GENIChomozygous130818480
1102965533102965534CT10GENICpossibly homozygous130843637