chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169574568169574569TG34GENIChomozygous108366131
1169578205169578206AG22GENIChomozygous108366133
1169586004169586005GA122GENICheterozygous108366135
1169586996169586997AC10GENIChomozygous108366137
1169587461169587462GT34GENIChomozygous108366139
1169588874169588875GA23GENIChomozygous108366141
1169589532169589533AG43GENIChomozygous108366143
1169590910169590911CT55GENIChomozygous108366145
1169590931169590932GT69GENICpossibly homozygous108366147