chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1239269637239269638A13GENIChomozygous127495564
1239270359239270360GC18GENIChomozygous109453163
1239270686239270686T21GENICheterozygous132265744
1239276692239276693GA29GENICheterozygous109205885
1239277036239277036GCG12GENIChomozygous134505300
1239277496239277499TTA10GENIChomozygous134172790
1239277788239277789TC3GENIChomozygous108585842
1239278068239278069C18GENIChomozygous127495568
1239279063239279064CA37GENIChomozygous108585845
1239279501239279502AG20GENIChomozygous109453165
1239281586239281587TC22GENIChomozygous108585846
1239288389239288389GC25GENIChomozygous127495571
1239291808239291809TA26GENIChomozygous108585859
1239294574239294575GA25GENIChomozygous108585863
1239296354239296357TTA18GENIChomozygous134172791
1239298218239298219TC22GENIChomozygous108585864
1239299083239299084AG22GENIChomozygous108585866
1239299194239299195TC23GENIChomozygous108585867
1239299705239299706GA29GENIChomozygous109453166
1239276713239276714A26GENICheterozygous131264837
1239276746239276746TTTCTTTTCTT31GENICheterozygous135140751
1239276748239276748T31GENICheterozygous135140752
1239276749239276750AT32GENICheterozygous135147221