chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173039939330399394GA21GENIChomozygous111241618
173039940330399404CG21GENIChomozygous111241620
173040048430400485GA33GENIChomozygous111241622
173040145330401454CG21GENIChomozygous111241624
173040230530402306TC15GENIChomozygous111241626
173040474530404746GA29GENIChomozygous111022192
173040482930404830CT27GENIChomozygous111189488
173040521530405216AG21GENIChomozygous111189490
173040539630405397AG11GENIChomozygous111189492
173040541630405417CT14GENIChomozygous111241628
173040567930405680GC20GENIChomozygous111022194
173040589830405899AG39GENIChomozygous111022196
173040596430405965GA33GENIChomozygous111189498
173040606630406067CT26GENIChomozygous111241630
173040741030407411TC22GENIChomozygous111022198
173040754030407541GA35GENIChomozygous111241632
173040829330408294GT34GENIChomozygous111241634
173040838530408386TG19GENIChomozygous111241636
173040867130408672AG12GENIChomozygous111241638
173040905130409052AC38GENIChomozygous111241640
173040932030409321TA10GENIChomozygous111241642
173041971930419720CT13GENIChomozygous111241646
173042010230420103TG26GENIChomozygous111189508
173042017030420171TC25GENIChomozygous111189510
173042020730420208TC25GENIChomozygous111189512
173042023230420233AT24GENIChomozygous111241648
173042055230420553TG13GENIChomozygous111022208
173042306930423070GT35GENIChomozygous111022214
173042311430423115CT28GENIChomozygous111022216
173042320930423210CT28GENIChomozygous111022218
173042327630423277TG31GENIChomozygous111022221
173042334230423343CT35GENIChomozygous111022223
173042353030423531TA22GENIChomozygous111022225
173042418430424185AG12GENIChomozygous111022227
173042553930425540TC28GENIChomozygous111241650
173042554930425550GC25GENIChomozygous111241652
173042565530425656GA23GENIChomozygous111241654
173042586230425863AG26GENIChomozygous111022229
173042598630425987AG29GENIChomozygous111022231
173042610430426105GA31GENIChomozygous111241656
173040981430409815CA2GENIChomozygous111600085