chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152399410723994108C31GENIChomozygous139622824
152399410723994108CA31GENICheterozygous403375301
152399742323997423TAAA37GENIChomozygous142458933
152400150424001509GTTTT53GENIChomozygous142458934
152400117824001179TC41GENIChomozygous142480994
152400169424001695GC59GENIChomozygous142480995
152400000524000006AG36GENIChomozygous142480992
152400117624001177GA41GENIChomozygous142480993
152400173224001738AAGACA60GENIChomozygous142458935
152400173924001739TGTGT60GENIChomozygous142458936
152400174124001742AG59GENIChomozygous142480996
152400174224001743CG59GENIChomozygous142480997
152400174324001744AT59GENIChomozygous142480998
152400209224002093CT46GENIChomozygous142480999
152400256024002561AG31GENIChomozygous142481000
152400425424004255GA50GENIChomozygous142481001
152400528124005281C28GENIChomozygous142458937
152400528224005283AC29GENIChomozygous142481002
152400632624006327AG10GENIChomozygous145871101
152400657924006580AG35GENIChomozygous142481003
152400752224007523TC40GENIChomozygous142481004
152400754024007541AG33GENIChomozygous142481005
152400820824008209AG29GENIChomozygous142481006
152400822324008254GGAGTCACAGCTTGCAAGGCAGGAGGCTGGA26GENIChomozygous142458938
152400883324008834TC50GENIChomozygous142481007
152400890924008910T40GENICpossibly homozygous142458939
152400899324008994AG30GENIChomozygous142481008
152400914124009142AG39GENIChomozygous142481009
152400946624009467GC36GENIChomozygous142481010
152400997224009973CT46GENIChomozygous142481011
152401050524010515CGCCGCCCCG30GENIChomozygous142458940
152400815824008159AG30GENIChomozygous154921945
152400815824008159A30GENICheterozygous403657414
152400817224008173GA26GENICheterozygous403907315
152400817224008173G26GENICpossibly homozygous403907314