chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7227094872270968GGACTGGGAAAAGGGCATTT9GENIChomozygous130611562
X7227351772273518A19GENICheterozygous130720007
X7232281972322819GC33GENIChomozygous129754431
X7232294172322941CTTTAGAAAGCCCTGTGTACCATCTGCTCATCCTCCTCGCCTCTGTCACCTCTCCTCTGAGTCCTTGGCAACCGCTAATCTTTTTAACAGTCTTTATACTTTCAC18GENICpossibly homozygous129754432