chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203029600203029600A12GENIChomozygous148211025
1203033607203033608C17GENIChomozygous135455304
1203034752203034753AG25GENIChomozygous135790590
1203035677203035678AG24GENIChomozygous135790592
1203037245203037246TA26GENIChomozygous148214045
1203033931203033932GA24GENIChomozygous148214042
1203034783203034784GA22GENIChomozygous148214043
1203036369203036370GA19GENIChomozygous148214044
1203037249203037250AG24GENIChomozygous148214046
1203037351203037352GA19GENIChomozygous148214047
1203037514203037515AG27GENIChomozygous135790593
1203037720203037721AG30GENIChomozygous135790594
1203038225203038226GA31GENIChomozygous135790596
1203038860203038861AG31GENIChomozygous135790597
1203040093203040094AG29GENIChomozygous135790598
1203040123203040124AG29GENIChomozygous135790599
1203040980203040981AG23GENIChomozygous135790602
1203041335203041336AG22GENIChomozygous135790603
1203041522203041523GA30GENIChomozygous148214048
1203042136203042137CT19GENIChomozygous135790605
1203042599203042600AG18GENIChomozygous135790606
1203043366203043367AG30GENIChomozygous135790607
1203043872203043873TA21GENIChomozygous148214049
1203044897203044898AG18GENIChomozygous148214050