chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115174238115174238T32GENIChomozygous128634264
8115174318115174319TC15GENIChomozygous116665614
8115174586115174587AT49GENIChomozygous116665616
8115174692115174693CA50GENIChomozygous116665618
8115174731115174732GC54GENIChomozygous116665620
8115175574115175575CA45GENIChomozygous116665622
8115176026115176027GA49GENIChomozygous116665624
8115176033115176034CA50GENIChomozygous116665626
8115176067115176068CT50GENIChomozygous116665628
8115176166115176167GA55GENIChomozygous116665630
8115176335115176336AG59GENIChomozygous116665632
8115176685115176686TC47GENIChomozygous116665634
8115176992115176992G38GENIChomozygous128634265
8115177625115177626AG48GENICpossibly homozygous116665636
8115177938115177939G17GENIChomozygous128634266
8115178271115178272GA41GENIChomozygous116665638
8115179325115179326GT45GENIChomozygous116665640
8115179326115179327TC45GENIChomozygous116665642
8115179363115179365AT50GENIChomozygous128634267
8115179482115179483CT40GENIChomozygous116665644
8115179509115179510TA36GENIChomozygous116665646