chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117442340974423410CT16GENIChomozygous139018928
117442608674426087T11GENICheterozygous138895378
117442614674426147CA18GENIChomozygous144903579
117442667074426671T14GENIChomozygous138895379
117442899574428996GA23GENIChomozygous139018929
117443157774431578GA14GENIChomozygous144903580
117443315174433152TG17GENIChomozygous144903581
117443332074433321AC22GENIChomozygous144903582
117443338474433385GA16GENIChomozygous144903583
117443339474433395AG14GENIChomozygous144903584
117443399174433992CT16GENIChomozygous144903585
117443401274434013CA17GENIChomozygous144903586
117443454074434541GC15GENIChomozygous144903587
117443472974434730TC15GENIChomozygous139018931
117443497374434974GA11GENIChomozygous139018932
117443529874435299GT14GENIChomozygous139018934
117443564874435649AG13GENIChomozygous139018935
117443572174435722AT9GENIChomozygous139018936
117443581474435815AC8GENIChomozygous139018938
117443591174435912AT15GENIChomozygous144903588
117443607274436073TA13GENIChomozygous144903589
117443664774436648CG11GENIChomozygous139018939
117443672074436721TA14GENIChomozygous144903590
117442960174429601AA4GENIChomozygous144881554
117442960574429605AGAGAG5GENIChomozygous144881555