chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174481814144818142CT29GENIChomozygous111054246
174481943644819437GA41GENIChomozygous111054248
174482017744820178TC29GENIChomozygous111054250
174482151944821520GA7GENIChomozygous111402481
174482659144826592GA6GENIChomozygous111054252
174482690444826905AC16GENIChomozygous111054254
174482851144828512CT27GENIChomozygous111054256
174482873544828736AG26GENIChomozygous111054258
174483132944831330TC32GENIChomozygous111054264
174483140244831403GA44GENIChomozygous111054266
174483329144833292TC37GENICpossibly homozygous111054268
174483739744837398AG9GENICheterozygous111402482
174483784444837845AG32GENIChomozygous111054270
174483923744839238CG33GENIChomozygous111054272
174482453744824538GA27GENIChomozygous111244836