chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99492841794928418GA27GENIChomozygous117391819
99492975994929760GA32GENIChomozygous117602767
99492991894929919AC29GENIChomozygous117602769
99493081994930820TC29GENIChomozygous117391826
99493139594931396TC29GENIChomozygous117391828
99493195194931952GC27GENIChomozygous117391830
99493252494932525GA36GENIChomozygous117602771
99493299194932992TC32GENIChomozygous117391831
99493302294933023TC24GENIChomozygous117391833
99493613494936135TC36GENIChomozygous117391837
99493625794936258AG28GENIChomozygous117391841
99493690994936910GA32GENIChomozygous117602773
99493696694936967GA32GENIChomozygous117602775
99493878094938781AG28GENIChomozygous117391844
99493988694939887TC29GENIChomozygous117391846
99493990094939901GA30GENIChomozygous117391848
99494008794940088CA33GENIChomozygous117602777
99494066494940665TC27GENIChomozygous117391850
99494270494942705TC30GENIChomozygous117391862
99494371394943714CT24GENIChomozygous117391866
99494390994943910GT32GENIChomozygous117391867
99494481394944814CA16GENIChomozygous117602781
99494569494945695CT34GENIChomozygous117602783
99494572094945721AT32GENIChomozygous117391869
99494593494945935GA32GENIChomozygous117391871
99494861594948616CT31GENIChomozygous117391890
99494865594948656TC32GENIChomozygous117391892
99494932594949326TG22GENIChomozygous117602789
99494980794949808AG18GENIChomozygous117391894
99494990094949901CT22GENIChomozygous117391896
99495011994950120AG12GENIChomozygous117391898
99495076694950767TC32GENIChomozygous117391900
99495129194951292CG21GENIChomozygous117602795
99495130394951304TC20GENIChomozygous117391901
99496557794965578CT48GENIChomozygous117391906
99496650494966505CA31GENIChomozygous117391908
99496662494966625CT32GENIChomozygous117391910
99496887294968873TC15GENIChomozygous117391913
99496958094969581TC31GENIChomozygous117391915
99497024094970241CT8GENIChomozygous117784937