chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166464602166464602TTCTCTTGGGGGTCTCCTCCACAGGTGTCCCAATTGCTCTCCCCTCTGGGCCCGCGTGCTTGTCATCGTCTGTCCACCCTCCTGGTCCCATTGCCTTGTCTCTTCCTCACCTTACCGCACCTCTTTCCCATCATCCTGACTCTCCATGTTTCCCTTACTAGATGTTGCCAAGGTCTGTCTGTCTGCCCAGCTGCC14GENICpossibly homozygous128269125
5166475625166475625C53GENIChomozygous128269126
5166493871166493883AGAGCAGAGAGC6GENICheterozygous128269127
5166510437166510437T53GENIChomozygous128269128
5166495529166495530AG59GENICheterozygous128303764
5166512788166512789C51GENIChomozygous128269129