chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1173382079173382080G-13GENIChomozygous825413567
1173383141173383142GA19GENICheterozygous825413568
1173383699173383700GA7GENIChomozygous825413569
1173383954173383955G-9GENICheterozygous825413570
1173384026173384027GA7GENICheterozygous825413571
1173385915173385916CT10GENICheterozygous825413572
1173386712173386714GG--9GENIChomozygous825413573
1173387165173387166GGA13GENIChomozygous825413574
1173387215173387216AG13GENIChomozygous825413575
1173387469173387470CT12GENICheterozygous825413576
1173387579173387580GA8GENIChomozygous825413577
1173387762173387763CT10GENIChomozygous825413578
1173388457173388458AG8GENIChomozygous825413579
1173389232173389233GA7GENIChomozygous825413580
1173389472173389473TC13GENICheterozygous825413581
1173389662173389663TC14GENIChomozygous825413582
1173389783173389784TA15GENIChomozygous825413583
1173389811173389812TC18GENICheterozygous825413584
1173389871173389872GA20GENIChomozygous825413585
1173390048173390049CG12GENIChomozygous825413586
1173390090173390091CT15GENIChomozygous825413587
1173390202173390203TC10GENIChomozygous825413588
1173390403173390404CT18GENIChomozygous825413589
1173390856173390857GA21GENIChomozygous825413590
1173391329173391330CA9GENIChomozygous825413591