chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4215489591215489592AG21GENIChomozygous57750093
4215490142215490143GGCACGTACGCACGCACGCACA2GENIChomozygous59060478
4215490823215490824AG8GENIChomozygous57750097
4215491066215491067TC2GENIChomozygous57750099
4215491314215491315GA14GENICpossibly homozygous57750101
4215491408215491409AG14GENIChomozygous57750103
4215491811215491812AATG4GENICheterozygous57750105
4215491828215491829CT13GENICpossibly homozygous59060480
4215492243215492244TC8GENIChomozygous57750107
4215492267215492268TC15GENIChomozygous57750109