chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106505209106505210CT13GENICheterozygous51765939
10106505225106505226AAGTGCAGTCTTGTGTGTGTGTGTGTGTGTGTGTG9GENICheterozygous52407365
10106505225106505226AAGTGCAGTCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG9GENICheterozygous52684117
10106506510106506511CA18GENICpossibly homozygous51590669