chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137937920379379204AT13GENIChomozygous115030555
137938026379380264AG11GENIChomozygous114689964
137938030279380303CT10GENIChomozygous114775249
137938030779380308AG10GENIChomozygous114775251
137938031179380312GA10GENIChomozygous114775253
137938064879380649GA17GENIChomozygous114402853
137938068579380686TG18GENIChomozygous115030557
137938092079380921CT19GENIChomozygous115030558
137938116379381164AC20GENIChomozygous114689970
137938176779381768AG19GENIChomozygous114402857
137938182679381827CT21GENIChomozygous114775259
137938232879382329GT15GENIChomozygous115030560
137938286279382863TC8GENIChomozygous114402859
137938311579383116AG15GENIChomozygous114689978
137938361479383615GA17GENIChomozygous114775263
137938428579384286TC19GENIChomozygous114689998
137938591679385917CT20GENICpossibly homozygous114775269
137938624679386247TC21GENIChomozygous114690014
137938636579386366CA9GENIChomozygous114690016
137938653279386533TC13GENIChomozygous114775271
137938751379387514CT20GENIChomozygous114775275
137938796079387961GA7GENIChomozygous114775277
137938838379388384TA9GENIChomozygous114690029
137938838479388385TG9GENIChomozygous114690030
137938864679388647TC9GENICpossibly homozygous114775279