chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18401905401906GT31GENIChomozygous110568465
18402029402030AC36GENIChomozygous110238775
18402045402046TC34GENIChomozygous110238777
18402070402071AG32GENIChomozygous110238779
18402400402401CT10GENIChomozygous110238784
18403232403233AG14GENIChomozygous110238786
18403406403407AG15GENIChomozygous110238788
18403431403432CT16GENIChomozygous110238790
18403922403923AG12GENIChomozygous110568468
18404064404065TC18GENIChomozygous110568471
18404195404196AG30GENIChomozygous110568474
18404307404308GA24GENIChomozygous110568477
18404475404476TG15GENIChomozygous110238792
18404598404599TC23GENIChomozygous110238794
18404635404636GC19GENIChomozygous110238796
18404851404852TC24GENIChomozygous110238800
18404888404889CT25GENIChomozygous110238802
18404891404892GA23GENIChomozygous110238804
18405078405079GA13GENIChomozygous110238806
18405617405618GA25GENIChomozygous110238809
18405675405676CT44GENIChomozygous110238811
18405683405684AG45GENIChomozygous110238813
18405869405870AG46GENIChomozygous110238815
18406106406107TA37GENIChomozygous110238817
18406136406137TC40GENIChomozygous110238819
18406184406185CT45GENIChomozygous110238821
18406344406345GT36GENIChomozygous110238823
18406360406361GA42GENIChomozygous110568479
18406728406729AG54GENIChomozygous110238825
18407014407015AG40GENIChomozygous110238831
18407488407489AT5GENIChomozygous110238837
18407703407704CT29GENIChomozygous110568482