chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166464602166464602TTCTCTTGGGGGTCTCCTCCACAGGTGTCCCAATTGCTCTCCCCTCTGGGCCCGCGTGCTTGTCATCGTCTGTCCACCCTCCTGGTCCCATTGCCTTGTCTCTTCCTCACCTTACCGCACCTCTTTCCCATCATCCTGACTCTCCATGTTTCCCTTACTAGATGTTGCCAAGGTCTGTCTGTCTGCCCAGCTGCC27GENICpossibly homozygous128269125
5166475625166475625C40GENIChomozygous128269126
5166510437166510437T51GENIChomozygous128269128
5166512788166512789C49GENIChomozygous128269129
5166495529166495530AG43GENICheterozygous128303764