chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118633051186330512GA37GENIChomozygous115927720
118633139886331399AG57GENIChomozygous115927722
118633198786331988AG53GENIChomozygous115927724
118633243786332438GA57GENIChomozygous115927726
118633449486334495AG42GENICpossibly homozygous115927728
118633569286335693CT68GENIChomozygous115927730
118634033986340340TC38GENIChomozygous115927732
118634058386340584TC39GENICpossibly homozygous115927734
118634079886340799AG52GENIChomozygous115927736
118634194586341946GT50GENIChomozygous115927738
118634360686343607TC58GENICpossibly homozygous115927740
118634385786343858GC51GENIChomozygous115927742
118634412986344130AG20GENIChomozygous118171346
118634423286344233AG60GENICheterozygous118171347
118634473486344735AG246GENICheterozygous118171348
118634552386345524TC69GENICpossibly homozygous115927744
118635036586350366TC52GENIChomozygous115927746
118634748186347482GT36GENICpossibly homozygous118188422
118634429586344296GA211GENICheterozygous118188420
118634489186344892AC73GENICheterozygous118188421