chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102941599102941600TC47GENIChomozygous109115427
1102944242102944243AG37GENIChomozygous109115429
1102945598102945599CT40GENIChomozygous109115433
1102946046102946047AG47GENIChomozygous120503647
1102946047102946048TA48GENIChomozygous120503648
1102947136102947137TA50GENIChomozygous109115435
1102947607102947608TC52GENIChomozygous109115437
1102947653102947654TA56GENIChomozygous109115439
1102947528102947528C55GENIChomozygous130818477
1102947579102947579C47GENIChomozygous130818478
1102948656102948656A37GENIChomozygous130818479
1102950349102950350CT55GENIChomozygous109115441
1102953494102953495CT42GENIChomozygous109115443
1102954626102954627CT45GENIChomozygous109115447
1102957497102957498TC57GENIChomozygous109115449
1102969965102969965AGGAGGAGG33GENIChomozygous130818480
1102965533102965534CT29GENICpossibly homozygous130843637
1102958021102958022AT50GENIChomozygous109115451
1102958165102958166CT48GENIChomozygous109115453
1102958201102958202AG48GENIChomozygous109115455
1102960758102960759AG45GENIChomozygous109115457
1102965291102965292TC46GENIChomozygous109115459
1102968260102968261TA54GENIChomozygous109115461