chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142901156142901157TG16GENIChomozygous54161995
7142901770142901771CA23GENIChomozygous54161996
7142901917142901918CT28GENIChomozygous54161997
7142902090142902091CT15GENICpossibly homozygous54161998
7142902888142902889TG22GENIChomozygous54162001
7142902892142902893TC22GENIChomozygous54162002
7142902912142902913CG18GENIChomozygous54162003
7142902965142902966CCTTTTTTT11GENIChomozygous55017835
7142903045142903046GT20GENIChomozygous54162005
7142903172142903173GA25GENIChomozygous54162006
7142904820142904821AT10GENIChomozygous54162007
7142905253142905254AG26GENIChomozygous54162008
7142905922142905923GA11GENIChomozygous54162011
7142906866142906867AG34GENIChomozygous54162012
7142906952142906953GA43GENIChomozygous54162013
7142907515142907516GA13GENIChomozygous54162014
7142909666142909681TTGTTGTTGTTGTTG---------------6GENIChomozygous55017837
7142909747142909748AG14GENIChomozygous54162019
7142910885142910894TTTTTTTTT---------10GENICheterozygous55017839
7142910886142910894TTTTTTTT--------10GENICpossibly homozygous55017841
7142910997142910998CCT15GENICpossibly homozygous54162021
7142911046142911047T-14GENIChomozygous54162022
7142911541142911542GA13GENIChomozygous54162023
7142911672142911678GTGTGT------7GENICheterozygous55017845
7142912010142912011GA24GENIChomozygous54162024
7142912852142912856TCTA----9GENIChomozygous54162026
7142913287142913288GT15GENIChomozygous54162039
7142914094142914095TTAG22GENIChomozygous54162040
7142915480142915481GA23GENIChomozygous54162044
7142916625142916626T-15GENICpossibly homozygous54924741
7142915102142915103AT22GENIChomozygous54803004
7142916076142916077AG15GENIChomozygous54803005