chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211543796211543797GA21GENIChomozygous108987489
1211544405211544406AC14GENIChomozygous108987490
1211544434211544435CT21GENIChomozygous108987491
1211544476211544477CG21GENIChomozygous108987492
1211544665211544666AG23GENIChomozygous108987493
1211545778211545779GA18GENIChomozygous108987495
1211545781211545782TC17GENIChomozygous108987496
1211546194211546195GT31GENIChomozygous108987497
1211546289211546290CT34GENIChomozygous108987498
1211546539211546540CT27GENIChomozygous108987499
1211547584211547585GA25GENIChomozygous108987500
1211547924211547925GC17GENIChomozygous108987503
1211548001211548002AG22GENIChomozygous108987504
1211549552211549553CA17GENIChomozygous108987505
1211549553211549554GT17GENIChomozygous108987506
1211549694211549695GA22GENIChomozygous108987507
1211553060211553061AT22GENIChomozygous108987508
1211554572211554573GA20GENIChomozygous108524267
1211556462211556463CT18GENIChomozygous108524273
1211556983211556984CT27GENIChomozygous108524275
1211559663211559664AG23GENIChomozygous108524277
1211560130211560131CT11GENIChomozygous108987512
1211560477211560478CT12GENIChomozygous108987513
1211560982211560983GA15GENIChomozygous108987514
1211562158211562159TC24GENIChomozygous108524284
1211563368211563369TG16GENIChomozygous108524292
1211566192211566193CG12GENIChomozygous108524298
1211566319211566320GA26GENIChomozygous108524300
1211566659211566660GC27GENIChomozygous108987515
1211566985211566986TC24GENIChomozygous108987516
1211567028211567029TC25GENIChomozygous108524304
1211567131211567132GT21GENIChomozygous108524306
1211568268211568269TA19GENIChomozygous108524308
1211569986211569987CT26GENIChomozygous108987519
1211571856211571857GA26GENIChomozygous108987520
1211572021211572022TC26GENIChomozygous108524310
1211574471211574472GA26GENIChomozygous108987522