chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130109605130109606AT19GENICpossibly homozygous116229350
7130112713130112714CT30GENIChomozygous116229351
7130113054130113055AC29GENICpossibly homozygous116229352
7130113542130113543AT26GENIChomozygous116229353
7130116743130116744TC29GENIChomozygous115889283
7130117965130117966AC21GENIChomozygous115889287
7130119067130119068CT21GENIChomozygous116229354
7130119485130119486GA37GENIChomozygous116229355
7130119796130119797CA34GENICpossibly homozygous116263929
7130120570130120571GA28GENIChomozygous116229356