chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124686257946862580AT10GENIChomozygous115342599
124686261146862612CT14GENIChomozygous115342601
124686296046862961CA11GENIChomozygous115342603
124686299946863000GT9GENIChomozygous115342605
124686306846863069CA16GENIChomozygous115397163
124686307246863073CG16GENIChomozygous115397165
124686311546863116AG23GENIChomozygous115397167
124686313146863132AG24GENIChomozygous115397169
124686317546863176AG20GENIChomozygous115397171
124686340946863410TC17GENIChomozygous115397173
124686373246863733CA19GENIChomozygous115397175
124686522846865229TA12GENIChomozygous115397177
124686544846865449TC3GENIChomozygous115495626
124686627046866271CT16GENIChomozygous115397179
124686923546869236TC17GENIChomozygous115342623
124687092646870927TC14GENIChomozygous115342625
124687130846871309TC4GENIChomozygous115342627
124687146546871466GA17GENIChomozygous115397187
124687150046871501TG18GENIChomozygous115342629
124687320546873206AG14GENIChomozygous115342635
124687421946874220AC22GENICpossibly homozygous115397189
124687422446874225AC23GENICpossibly homozygous115397191
124687543546875436AG8GENIChomozygous115342637
124687610746876108CT15GENIChomozygous115342639