chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X159722415159722416TA6GENIChomozygous974439338
X159722697159722698TG11GENIChomozygous974439339
X159724467159724468CT9GENIChomozygous974439340
X159724631159724632TC8GENIChomozygous974439341
X159728185159728186TC7GENIChomozygous974439342
X159740702159740703AT3GENIChomozygous974439343
X159747310159747311AT7GENIChomozygous974439344
X159749126159749127AG8GENIChomozygous974439345
X159749663159749664GT10GENIChomozygous974439346
X159749849159749850GT9GENIChomozygous974439347
X159750543159750544GA9GENIChomozygous974439348
X159753355159753356GT7GENIChomozygous974439349
X159753519159753520GA7GENIChomozygous974439350
X159754146159754147CT10GENIChomozygous974439351
X159754168159754169GA12GENIChomozygous974439352
X159754713159754714GA5GENIChomozygous974439353
X159755618159755619GT4GENIChomozygous974439354
X159756648159756649CT3GENIChomozygous974439355
X159757038159757039CT11GENIChomozygous974439356
X159757581159757582GC4GENIChomozygous974439357
X159757618159757619CG6GENICheterozygous974439358
X159758810159758811AG9GENIChomozygous974439359
X159760584159760585CG9GENIChomozygous974439360
X159760932159760933GA3GENIChomozygous974439361
X159760971159760972TC9GENIChomozygous974439362
X159797449159797450AG6GENIChomozygous974439363
X159825256159825257TC3GENIChomozygous974439364
X159825495159825496AG5GENIChomozygous974439365
X159825498159825499AC5GENIChomozygous974439366
X159825764159825765AG3GENIChomozygous974439367
X159826229159826230GA4GENIChomozygous974439368
X159826947159826948CG4GENIChomozygous974439369
X159827657159827658TG11GENIChomozygous974439370
X159827888159827889AT8GENIChomozygous974439371
X159829190159829191TA12GENIChomozygous974439372
X159829925159829926TG22GENIChomozygous974439373
X159830176159830177CA12GENIChomozygous974439374
X159834823159834824TC2GENIChomozygous974439375
X159835042159835043GC9GENIChomozygous974439376
X159837388159837389AG12GENIChomozygous974439377