chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18402029402030AC13GENIChomozygous110238775
18402045402046TC15GENIChomozygous110238777
18402070402071AG12GENIChomozygous110238779
18402400402401CT6GENIChomozygous110238784
18404064404065TC7GENIChomozygous110568471
18404307404308GA10GENIChomozygous110568477
18404475404476TG13GENIChomozygous110238792
18403232403233AG12GENIChomozygous110238786
18403406403407AG3GENIChomozygous110238788
18403431403432CT2GENIChomozygous110238790
18404598404599TC6GENIChomozygous110238794
18404635404636GC7GENIChomozygous110238796
18404851404852TC11GENIChomozygous110238800
18404888404889CT9GENIChomozygous110238802
18404891404892GA9GENIChomozygous110238804
18405078405079GA7GENIChomozygous110238806
18405617405618GA16GENIChomozygous110238809
18405675405676CT20GENIChomozygous110238811
18405683405684AG19GENIChomozygous110238813
18406106406107TA15GENIChomozygous110238817
18406136406137TC23GENIChomozygous110238819
18406184406185CT23GENIChomozygous110238821
18406344406345GT14GENIChomozygous110238823
18406360406361GA17GENIChomozygous110568479
18406728406729AG10GENIChomozygous110238825
18406825406826AC12GENIChomozygous110238827
18406828406829GA13GENIChomozygous110238829
18407014407015AG4GENIChomozygous110238831
18406792406793GC15GENIChomozygous110669612
18407228407229TC9GENIChomozygous110238835
18407533407534CT2GENIChomozygous110619407