chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171581456415814565AG17GENIChomozygous110968432
171582074315820744AG27GENIChomozygous110968454
171582085315820854GA22GENIChomozygous111402142
171582109115821092AC19GENIChomozygous111402143
171582128815821289CT31GENIChomozygous110968456
171582179915821800TA27GENIChomozygous111172263
171582231015822311GA29GENIChomozygous110968460
171582236815822369TC23GENIChomozygous110968462
171582245615822457CT12GENIChomozygous110968464
171582252715822528TC13GENIChomozygous110968466
171582252815822529GA13GENIChomozygous110968468
171582417015824171AC10GENIChomozygous110968474
171582426415824265TC8GENIChomozygous111172271
171582490315824904CG35GENIChomozygous110968476
171582499715824998GA26GENIChomozygous111172273
171582516715825168TC32GENIChomozygous110968478
171582567315825674CT22GENIChomozygous111172275
171582650915826510TC27GENIChomozygous110968482
171582671415826715TA14GENIChomozygous110968486
171582712715827128CG31GENIChomozygous110968488
171582924015829241GA23GENIChomozygous110968502
171582931415829315TC14GENIChomozygous110968504
171582938115829382GA14GENIChomozygous110968506
171582959415829595AG16GENIChomozygous110968508
171582972515829726TC20GENIChomozygous110968512
171582980815829809GA20GENIChomozygous110968514
171582993115829932GA18GENIChomozygous111172277
171582997015829971AG19GENIChomozygous111172279
171582999615829997GA26GENIChomozygous111172281
171583019915830200GA29GENICpossibly homozygous111172283
171583022615830227TC28GENIChomozygous111172285