chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73021528030215281GA19GENIChomozygous116133785
73021545030215451TA23GENIChomozygous116133787
73021567830215679AG18GENIChomozygous116133789
73021594930215950TC27GENIChomozygous116133791
73021611430216114ACACACAA13GENIChomozygous132652574
73021620730216208TC25GENIChomozygous116133793
73021621830216219AT25GENIChomozygous116133795
73021648630216487GA13GENIChomozygous116133797
73021725430217255CG11GENIChomozygous116133799
73021731930217320AG18GENIChomozygous116133801
73021747130217472TC13GENIChomozygous116133803
73021768030217681AG24GENIChomozygous116133805
73021805230218053GA26GENIChomozygous116133807
73021850930218510A23GENIChomozygous132652576
73021931030219311GT29GENIChomozygous116133811
73021980230219803AT19GENIChomozygous116133815
73022024330220244TA13GENIChomozygous116133817
73022084630220847GT24GENIChomozygous116133819
73022166030221661AG20GENIChomozygous116133821
73022264530222646AC15GENIChomozygous116133823
73022401630224017CT19GENIChomozygous116133825
73021625930216270CTTCCTTCCTT31GENIChomozygous135328155
73021992530219926C27GENIChomozygous135328156
73022218130222190CATCATCAA21GENICpossibly homozygous135328157
73021785930217860CA20GENIChomozygous126656313
73022042030220421GA21GENIChomozygous126656314
73022385830223859CT19GENIChomozygous126656316
73022342430223424G24GENIChomozygous131010353
73022342630223426AG23GENIChomozygous131010354
73022443130224432AC17GENIChomozygous116133827
73022446930224470CA19GENIChomozygous126656317
73022593830225939AC15GENIChomozygous126656318
73022847330228473CAT22GENIChomozygous131010355
73022850730228508CT26GENIChomozygous126656320
73022865730228658AC13GENIChomozygous126656321
73022887230228873TA20GENIChomozygous116133844
73022889730228898AG21GENIChomozygous116133846
73022913130229132GA18GENIChomozygous126656322
73022924730229248TC24GENIChomozygous116133850
73022952430229525TC23GENIChomozygous118276670
73022963830229639CT21GENIChomozygous116133858
73026601830266025GATAGAT16GENIChomozygous135328158