chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1257077030257077031TG18GENIChomozygous108623106
1257077701257077702AG20GENIChomozygous108623108
1257077862257077863AC18GENICpossibly homozygous108623109
1257078503257078504GA31GENIChomozygous109024291
1257078554257078555G30GENIChomozygous131267045
1257078851257078852TC17GENIChomozygous108623116
1257079206257079207TC17GENIChomozygous108623117
1257079207257079208GA17GENIChomozygous109024294
1257079813257079814TC20GENIChomozygous108623118
1257080487257080488AT22GENIChomozygous108623119
1257080948257080949TC18GENIChomozygous109024296
1257081344257081345GA22GENIChomozygous108623122
1257081669257081670AT24GENIChomozygous108623123
1257081708257081709AG29GENIChomozygous108623124
1257081709257081710AC29GENIChomozygous108623125
1257082007257082008TC27GENIChomozygous108623126
1257082334257082335TC29GENIChomozygous108623127
1257078721257078721GTTGGAGCACAGGG19GENIChomozygous127505767