chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106505209106505210CT20GENICheterozygous51765939
10106505225106505226AAGTGCAGTCTTGTGTGTGTGTGTGTGTGTGTGTG14GENICpossibly homozygous52407365
10106506510106506511CA10GENIChomozygous51590669