chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115451265115451266TC4GENIChomozygous52826089
8115451380115451381CG8GENIChomozygous52826090
8115451567115451568AAG17GENIChomozygous52826091
8115452053115452054CT29GENIChomozygous52826092
8115452637115452638CT37GENIChomozygous52826093
8115453743115453744CCT14GENICheterozygous52826095
8115455587115455588TTACACACACAC4GENICheterozygous53411106
8115455587115455588TTACACACACACAC4GENICheterozygous53411107
8115457901115457902AG23GENIChomozygous52826100
8115458185115458186CT36GENIChomozygous52826102
8115458699115458700CCT24GENICpossibly homozygous52826104
8115459272115459273T-20GENICpossibly homozygous53305523
8115457762115457763AAC12GENIChomozygous53167553
8115458425115458426A-24GENIChomozygous53167555
8115460283115460284GA25GENIChomozygous53050191
8115453729115453730AAT14GENIChomozygous53050185