chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142900429142900430AG24GENIChomozygous54161994
7142901156142901157TG22GENICpossibly homozygous54161995
7142901770142901771CA20GENIChomozygous54161996
7142901917142901918CT23GENIChomozygous54161997
7142902086142902087TTATCTATCC12GENIChomozygous55100918
7142902249142902250TC18GENIChomozygous54162000
7142902888142902889TG27GENIChomozygous54162001
7142902892142902893TC25GENIChomozygous54162002
7142902912142902913CG23GENIChomozygous54162003
7142902965142902966CCTCTCT8GENIChomozygous54162004
7142903045142903046GT37GENIChomozygous54162005
7142903172142903173GA22GENIChomozygous54162006
7142904820142904821AT22GENIChomozygous54162007
7142905253142905254AG31GENIChomozygous54162008
7142905675142905681CCCCCC------6GENICheterozygous54162009
7142905676142905681CCCCC-----6GENICheterozygous54162010
7142905922142905923GA19GENIChomozygous54162011
7142906866142906867AG29GENIChomozygous54162012
7142906952142906953GA31GENIChomozygous54162013
7142907515142907516GA22GENIChomozygous54162014
7142909666142909681TTGTTGTTGTTGTTG---------------9GENIChomozygous55017837
7142909747142909748AG21GENIChomozygous54162019
7142910885142910894TTTTTTTTT---------8GENICheterozygous55017839
7142910886142910894TTTTTTTT--------8GENICheterozygous55017841
7142910997142910998CCT20GENICpossibly homozygous54162021
7142911046142911047T-24GENIChomozygous54162022
7142911541142911542GA26GENIChomozygous54162023
7142911672142911678GTGTGT------1GENIChomozygous55017845
7142912010142912011GA24GENIChomozygous54162024
7142912682142912683TTAC7GENICheterozygous54162025
7142912682142912683TTACACAC7GENICpossibly homozygous55017847
7142913287142913288GT26GENIChomozygous54162039
7142914094142914095TTAG24GENIChomozygous54162040
7142914478142914479AAGGGCTAGCTGTTTT33GENIChomozygous54162041
7142914977142914978GA28GENIChomozygous54162043
7142915480142915481GA22GENICpossibly homozygous54162044
7142916625142916626T-25GENICpossibly homozygous54924741
7142916624142916626TT--25GENICheterozygous55032362