chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116932740169327402AG20GENIChomozygous115894644
116932750469327505TG13GENIChomozygous116267057
116932858969328590CT19GENIChomozygous115981133
116932966769329668TC21GENIChomozygous115894648
116933024069330241TC5GENIChomozygous115981135
116933030269330303TC6GENIChomozygous115981137
116933159969331600AT22GENIChomozygous115981139
116933164969331650CA22GENIChomozygous115894650
116933215769332158AG22GENIChomozygous115894654
116933238569332386CG21GENIChomozygous115894656
116933474869334749AT15GENIChomozygous115981141
116933540169335402TC15GENIChomozygous115894664
116933819669338197CT27GENIChomozygous115981143
116933847069338471TC27GENIChomozygous115981145
116933975869339759CT18GENIChomozygous115981147
116934006369340064GA15GENIChomozygous115981149
116934022769340228CT20GENIChomozygous115894678
116934056569340566CT15GENIChomozygous115981151
116934199869341999TA23GENIChomozygous115894682
116934307069343071AG28GENIChomozygous115981153
116934377469343775TG23GENIChomozygous115981155
116934384469343845CT14GENIChomozygous115981157
116934407969344080AC21GENICpossibly homozygous115981159
116934828069348281TC21GENIChomozygous115981161
116935043069350431TC31GENIChomozygous115894690
116933372969333730CT12GENIChomozygous116049435
116933446869334469GA13GENIChomozygous116049437
116935235169352352AG27GENIChomozygous115894692
116935249969352500AG18GENIChomozygous115894694
116935356569353566TC14GENIChomozygous115894696
116935459969354600GA20GENIChomozygous115894700
116935462369354624AG25GENIChomozygous115894702
116935465769354658GA22GENIChomozygous115981165
116935474569354746AG27GENIChomozygous115981167
116935549169355492CA14GENIChomozygous115981169
116935563269355633GA18GENIChomozygous115894710
116935476569354766AG14GENIChomozygous115894704
116935476669354767TC14GENIChomozygous115894706