chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120796589120796590AT18GENIChomozygous115857082
7120798005120798006TC20GENIChomozygous115857084
7120798854120798855CT40GENICheterozygous115857086
7120799107120799108CA20GENIChomozygous118360364
7120800362120800363AC26GENIChomozygous118407019
7120801425120801426GA9GENIChomozygous115857106
7120801474120801475CT10GENIChomozygous115857108
7120802152120802153CT13GENIChomozygous115857110
7120802372120802373GT9GENIChomozygous115857112
7120809575120809576AC12GENIChomozygous115857124
7120809661120809662CA21GENIChomozygous115857126
7120809733120809734GT21GENIChomozygous115857128
7120809741120809742AG21GENIChomozygous118259127
7120809742120809743GC19GENIChomozygous116393648
7120810076120810077TA17GENIChomozygous118259129
7120810077120810078AG17GENIChomozygous118259131
7120810302120810303AG21GENIChomozygous115857130
7120822124120822125GA13GENIChomozygous115857132
7120826719120826720AG10GENICpossibly homozygous115857134
7120826754120826755GT15GENIChomozygous115857136
7120832734120832735AG17GENIChomozygous118286344
7120832888120832889TC21GENIChomozygous115857138