chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171581456415814565AG31GENIChomozygous110968432
171582074315820744AG30GENIChomozygous110968454
171582128815821289CT35GENIChomozygous110968456
171582231015822311GA25GENIChomozygous110968460
171582236815822369TC29GENIChomozygous110968462
171582245615822457CT20GENICpossibly homozygous110968464
171582252715822528TC20GENIChomozygous110968466
171582252815822529GA20GENIChomozygous110968468
171582289415822895TG27GENIChomozygous110968470
171582351315823514TG33GENIChomozygous111172269
171582179915821800TA34GENIChomozygous111172263
171582261015822611TC11GENIChomozygous111172265
171582109115821092AC42GENIChomozygous111402143
171582106415821065AG35GENIChomozygous119331723
171582358015823581A35GENIChomozygous129427523
171582417015824171AC27GENIChomozygous110968474
171582418915824189T25GENICpossibly homozygous129427524
171582426415824265TC13GENIChomozygous111172271
171582490315824904CG47GENIChomozygous110968476
171582499715824998GA35GENIChomozygous111172273
171582516715825168TC27GENIChomozygous110968478
171582526915825270CT38GENIChomozygous110968480
171582567315825674CT35GENIChomozygous111172275
171582650915826510TC27GENIChomozygous110968482
171582671415826715TA26GENIChomozygous110968486
171582712715827128CG34GENIChomozygous110968488
171582924015829241GA29GENIChomozygous110968502
171582931415829315TC33GENIChomozygous110968504
171582938115829382GA32GENIChomozygous110968506
171582959415829595AG34GENIChomozygous110968508
171582972515829726TC30GENIChomozygous110968512
171582980815829809GA32GENIChomozygous110968514
171582993115829932GA32GENIChomozygous111172277
171582997015829971AG27GENIChomozygous111172279
171582999615829997GA31GENIChomozygous111172281
171583019915830200GA49GENIChomozygous111172283
171583022615830227TC44GENIChomozygous111172285
171583026615830266A34GENIChomozygous132214410