chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104492716044927161AG43GENIChomozygous534204156
104493287844932897GCACCCCCTTCTCTCACAA-------------------12GENIChomozygous696046997
104493478244934783GA31GENICheterozygous536878981
104493614544936146GA52GENIChomozygous534204157
104493625244936253T-30GENIChomozygous696046998
104493741344937414TTACAC11GENICpossibly homozygous696046999
104493825844938259AG32GENIChomozygous534204158
104493825944938260AG36GENICpossibly homozygous534204159
104493829144938292CCTTT9GENIChomozygous696047001
104494024544940246CA56GENIChomozygous534204160
104494136044941361TC55GENIChomozygous534204161
104494158544941586AG39GENICheterozygous534204162
104494200444942005GA49GENIChomozygous536878982
104494290544942906CT78GENIChomozygous534204163