chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142901156142901157TG32GENIChomozygous54161995
7142901770142901771CA24GENIChomozygous54161996
7142901917142901918CT29GENIChomozygous54161997
7142902086142902087TTATCTATCC4GENIChomozygous55100918
7142902249142902250TC31GENIChomozygous54162000
7142902888142902889TG31GENIChomozygous54162001
7142902892142902893TC28GENIChomozygous54162002
7142902912142902913CG20GENIChomozygous54162003
7142902965142902966CCTCTCT14GENIChomozygous54162004
7142903045142903046GT29GENIChomozygous54162005
7142903172142903173GA29GENIChomozygous54162006
7142904820142904821AT26GENIChomozygous54162007
7142905253142905254AG26GENIChomozygous54162008
7142905675142905681CCCCCC------3GENICheterozygous54162009
7142905676142905681CCCCC-----3GENICheterozygous54162010
7142905922142905923GA33GENIChomozygous54162011
7142906866142906867AG32GENIChomozygous54162012
7142906952142906953GA23GENIChomozygous54162013
7142907515142907516GA24GENIChomozygous54162014
7142909666142909681TTGTTGTTGTTGTTG---------------2GENIChomozygous55017837
7142909747142909748AG13GENIChomozygous54162019
7142910885142910894TTTTTTTTT---------13GENICheterozygous55017839
7142910886142910894TTTTTTTT--------13GENICpossibly homozygous55017841
7142910997142910998CCT20GENICpossibly homozygous54162021
7142911046142911047T-34GENIChomozygous54162022
7142911336142911337GGA1GENIChomozygous55100920
7142911541142911542GA26GENIChomozygous54162023
7142912010142912011GA25GENIChomozygous54162024
7142912682142912683TTACACAC3GENIChomozygous55017847
7142913287142913288GT26GENIChomozygous54162039
7142914094142914095TTAG20GENIChomozygous54162040
7142914478142914479AAGGGCTAGCTGTTTT25GENIChomozygous54162041
7142915480142915481GA20GENIChomozygous54162044
7142916624142916626TT--22GENIChomozygous55032362
7142918123142918124G-10GENIChomozygous55883163
7142916076142916077AG33GENIChomozygous54803005
7142916911142916912AG19GENIChomozygous55883159
7142917456142917457AT20GENIChomozygous55883161