chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
66021877160218772CT6GENIChomozygous54433427
66021999860219999T-3GENICheterozygous54433431
66022242060222421TC30GENIChomozygous54433433
66022331960223320GA28GENICpossibly homozygous54433435
66022341560223416TC19GENIChomozygous54433437
66022443760224438G-18GENIChomozygous54433439
66022480860224809CA21GENIChomozygous54433441
66022490660224907CA17GENIChomozygous54433443
66022512060225121CG18GENICheterozygous54433445
66022569960225700GT22GENICpossibly homozygous54433455
66022584460225845AG21GENICpossibly homozygous54433457
66022594460225945TC22GENIChomozygous54433459
66022601160226098GTATCTCCCTATGTAGCTCAGGCTAGACTTAAACTCATGATTCTCTTGTCTGAGCTTCCTGAAGGCTGGGATGACAGGTAAGGACAG---------------------------------------------------------------------------------------2GENIChomozygous55507290
66022618860226189CT3GENIChomozygous54433465
66022619860226199TC8GENIChomozygous54433467
66022658160226582CA9GENIChomozygous54433469
66022661560226616GA6GENIChomozygous54433471
66022661760226618AG7GENIChomozygous54433473
66022703860227039GC6GENIChomozygous54433475
66022759660227597CA14GENIChomozygous54433481
66022771360227714TC18GENICpossibly homozygous54433483
66022801060228011GA24GENICpossibly homozygous54433485
66022805760228058CT22GENICpossibly homozygous54433487
66022828260228283TC13GENICpossibly homozygous54433489
66022851360228514GA20GENICpossibly homozygous54433491
66022856260228563TC13GENICpossibly homozygous54433493
66022861560228616T-2GENIChomozygous54433495
66022869060228691GA3GENIChomozygous54433497
66022894460228945CT10GENIChomozygous54433499
66022940060229405TTCTG-----5GENIChomozygous54433501
66022987560229876AAAAGG4GENIChomozygous54433503
66022990360229907AAAG----1GENIChomozygous54433505
66023018560230186GA14GENIChomozygous54433511
66023045760230458AG8GENICheterozygous54433513
66023100560231006AG6GENIChomozygous54433515