chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9121155928121155929GGTTT15GENIChomozygous52311403
9121155954121155955T-12GENICpossibly homozygous52311404
9121158838121158842ACGT----19GENIChomozygous52311405
9121158890121158891TC15GENIChomozygous52156840
9121160081121160082TA24GENIChomozygous52156842
9121160475121160476GA25GENIChomozygous52311406
9121162078121162079AAAC7GENICheterozygous52156844
9121165895121165896TC22GENIChomozygous52311407
9121173502121173503AG22GENIChomozygous52156852
9121174033121174034CCAAG25GENIChomozygous52156854