chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X6862606568626066GC26GENICpossibly homozygous108448350
X6863109968631100TC20GENIChomozygous108448352
X6863129268631293CT34GENIChomozygous108448354
X6863153768631538AG25GENIChomozygous108448356
X6863198968631990GA19GENIChomozygous108448358
X6863238268632383GC26GENIChomozygous108448360
X6863292968632930CT25GENIChomozygous108448362
X6863355268633553AG17GENIChomozygous108448364
X6863397568633976GC18GENIChomozygous108448366
X6863501468635015AG13GENIChomozygous108448368
X6863644668636447CT19GENIChomozygous108448370
X6863675568636756CT16GENIChomozygous108448372
X6863760068637601CA13GENIChomozygous108448374