chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203826226203826227GGTTTTT18GENICpossibly homozygous61584491
1203826237203826238TTTTTTTTTC12GENICheterozygous61584492
1203828478203828479TA27GENICheterozygous61060800
1203828480203828481TA28GENICheterozygous61060801
1203831669203831670GT53GENICpossibly homozygous62029450
1203831939203831940GA51GENIChomozygous62029451
1203833309203833310TC42GENIChomozygous61060803
1203835250203835251CT35GENIChomozygous62029452
1203835292203835293AG35GENIChomozygous61060805
1203837516203837517GA46GENICpossibly homozygous61060806
1203839461203839462CT55GENIChomozygous62029453
1203840224203840225TG54GENIChomozygous62029454
1203840450203840451CT44GENIChomozygous62029455