chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108812071588120716AAT2GENIChomozygous51534467
108812104288121043AACAGGGTTTCTCTTGTAG14GENIChomozygous52205791
108812118788121188GA27GENIChomozygous52205793
108812119688121197TC26GENIChomozygous52205795
108812128988121290CT21GENIChomozygous52205797
108812166388121664CA22GENIChomozygous52205799
108812167688121677GA20GENIChomozygous52205801
108812183488121835CCT13GENICpossibly homozygous51924808
108812185088121851C-19GENICheterozygous51534468
108812211988122120AG31GENIChomozygous52205803
108812224588122246C-8GENIChomozygous52205805
108812227088122271AAT2GENIChomozygous52164752
108812244188122442AG21GENIChomozygous52205807
108812270788122711TACA----11GENIChomozygous52205809
108812275488122755CCTTT20GENIChomozygous52205811
108812285788122858CA24GENIChomozygous52205813
108812310788123108AG12GENIChomozygous52205815
108812326888123269TC30GENIChomozygous52205817
108812327188123273CA--28GENIChomozygous52205819
108812334788123348TC15GENIChomozygous52205821
108812337788123378CG18GENIChomozygous52205823
108812337988123380CT18GENIChomozygous52205825
108812350788123508AT11GENICpossibly homozygous52205827
108812355988123560AT5GENIChomozygous52205829
108812357188123572CCT4GENIChomozygous52205831
108812357588123576GGGCTGGGGATTGA4GENIChomozygous52205833
108812368988123693AGAA----6GENIChomozygous52205835
108812381288123813TC12GENIChomozygous52205837
108812640388126404TC15GENIChomozygous52205839
108812641688126417AAT11GENIChomozygous52205841
108812642288126423GGT6GENICheterozygous51534469
108812643488126437TTG---10GENICheterozygous52205843
108812651588126516AG14GENIChomozygous52205845
108812664688126648GT--7GENIChomozygous52205847
108812689288126893GT25GENICheterozygous52205849
108812692688126927CG17GENIChomozygous52205851
108812801988128020AT22GENIChomozygous52205853
108812804788128048GA29GENICpossibly homozygous52205855
108813034888130349CT26GENIChomozygous52205857
108813054688130547CT22GENIChomozygous52205859
108813088288130883GA20GENIChomozygous52205861