chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115174586115174587AT24GENIChomozygous116665616
8115174692115174693CA19GENIChomozygous116665618
8115174731115174732GC23GENIChomozygous116665620
8115175574115175575CA19GENIChomozygous116665622
8115176026115176027GA19GENIChomozygous116665624
8115176033115176034CA22GENIChomozygous116665626
8115176335115176336AG16GENIChomozygous116665632
8115176685115176686TC21GENIChomozygous116665634
8115176992115176992G12GENICpossibly homozygous128634265
8115177625115177626AG14GENIChomozygous116665636
8115177938115177939G5GENICheterozygous128634266
8115179325115179326GT11GENIChomozygous116665640
8115179326115179327TC11GENIChomozygous116665642
8115179363115179365AT12GENIChomozygous128634267
8115179482115179483CT11GENIChomozygous116665644
8115179509115179510TA9GENIChomozygous116665646