chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263448854263448855CT29GENIChomozygous108633073
1263450387263450388AG12GENIChomozygous108633075
1263452001263452002TA41GENIChomozygous108633079
1263452452263452453GA32GENIChomozygous108633081
1263453135263453136AG27GENIChomozygous108633083
1263455588263455589AT30GENIChomozygous108633087
1263458131263458132TG24GENIChomozygous108633093
1263459229263459230GA32GENIChomozygous108633095
1263459234263459235GC30GENIChomozygous108633097
1263461297263461298AG18GENIChomozygous108633113
1263461432263461433CT29GENIChomozygous108633114
1263463258263463259CT27GENIChomozygous108633116
1263466568263466569CT20GENIChomozygous108633118
1263466863263466864AG19GENIChomozygous108633120
1263466864263466865GT19GENIChomozygous108633122
1263466987263466988TG29GENIChomozygous108633124
1263467003263467004CT33GENIChomozygous108633126
1263467041263467042CG25GENIChomozygous108633128
1263467593263467594AG32GENIChomozygous108633130
1263467846263467847CT23GENIChomozygous108633132
1263469726263469727GA42GENIChomozygous108633154
1263469762263469763AG44GENIChomozygous108633156
1263469790263469791GA39GENIChomozygous108633158
1263469803263469804GA35GENIChomozygous108633160
1263469905263469906CG24GENIChomozygous108633162
1263470132263470133GC25GENIChomozygous108633164
1263470138263470139TC24GENIChomozygous108633166
1263470449263470450CT36GENIChomozygous108633168
1263470464263470465CT30GENIChomozygous108633170
1263470531263470532TC12GENIChomozygous108633172
1263470736263470737TC20GENIChomozygous108633174
1263470824263470825GA33GENIChomozygous108633176
1263472263263472264CT15GENIChomozygous108633178
1263472698263472699TA14GENIChomozygous108633180