chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91664778016647781AT14GENIChomozygous117681520
91664897416648975AC30GENIChomozygous117681522
91664907516649076TC32GENIChomozygous117681524
91664981216649813CT25GENIChomozygous117269593
91665011416650115AG22GENIChomozygous117681526
91665012616650127CG21GENIChomozygous117681528
91665049316650494TG16GENIChomozygous117681530
91665133816651339AC22GENIChomozygous117681532
91665140116651402TC22GENIChomozygous117674321
91665151416651515CT27GENIChomozygous117681534
91665251616652517CT24GENIChomozygous117681536
91665275716652758CA18GENIChomozygous117681538
91665278216652783TC23GENIChomozygous117681540
91665329816653299CT37GENIChomozygous117681542
91665336516653366AT28GENIChomozygous117681544
91665392916653930TG16GENIChomozygous117681546
91665464516654646CT33GENIChomozygous117681548
91665491616654917GA28GENIChomozygous117681550
91665515016655151AG23GENIChomozygous117681552
91665529616655297GA27GENIChomozygous117681554
91665546016655461CT40GENIChomozygous117681556
91665573116655732TC33GENIChomozygous117681558
91665630616656307CT34GENIChomozygous117681560
91665632416656325CT38GENIChomozygous117681562
91665635816656359CT39GENIChomozygous117681564
91665694016656941TC32GENIChomozygous117681566
91665780216657803AG24GENIChomozygous117681568
91665781016657811GA24GENIChomozygous117681570
91665787516657876CT20GENIChomozygous117681572
91665794416657945TC26GENIChomozygous117681574
91665813716658138CT32GENIChomozygous117681576
91665836616658367CT29GENIChomozygous117681578
91665850316658504TC26GENIChomozygous117681580
91665859816658599TC23GENIChomozygous117681582
91665861816658619CT24GENIChomozygous117681584
91666032216660323AG34GENIChomozygous117681586
91666086116660862CT21GENIChomozygous117681588
91666089316660894CT24GENIChomozygous117681590
91666121816661219TC24GENIChomozygous117269598
91666122416661225CA23GENIChomozygous117681592
91666127116661272AC15GENIChomozygous117681594