chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153315669333156694CT59GENIChomozygous112671875
153315672833156729GC57GENIChomozygous112671877
153315673533156736AC54GENIChomozygous112671879
153315734033157341GA70GENIChomozygous112671881
153315747133157472CT61GENIChomozygous112671883
153315778733157788GA43GENIChomozygous112671885
153315791533157916GA64GENIChomozygous112671887
153315895933158960GT58GENIChomozygous112671889
153315914633159147TC67GENIChomozygous112671891
153315932533159326G62GENIChomozygous131159162
153315751633157516TCAAAATAT35GENIChomozygous135220475
153315751833157518ACAGTGAGCAAGGACACAGTGAGT30GENIChomozygous135220476
153315752133157521ATGAGCATGTACAGGGAGCCACGAAAGCACTTAGGAGGAAGACAGCCTATTCTAGGAGGTCA23GENIChomozygous135220477
153315898433158984AGAC51GENICpossibly homozygous131159161
153315975533159756GT56GENIChomozygous112671893
153315981933159820TC56GENIChomozygous112671894
153315991633159916A56GENIChomozygous131159163
153316032033160321TG83GENIChomozygous112671896
153316057733160578TC50GENIChomozygous112671898
153316172333161724AG64GENIChomozygous112671900
153316175633161757GA57GENIChomozygous112671902
153316183333161834CA64GENIChomozygous112671904
153316489933164899AGAA52GENIChomozygous131159164
153316524733165248CT59GENIChomozygous112671906