chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28180681481806815CA23GENIChomozygous58907426
28180706881807069TG21GENIChomozygous58907427
28180716381807164GA21GENIChomozygous58907428
28180765981807660GA16GENIChomozygous58907429
28180798181807982AAAAAGAAAG12GENIChomozygous60751656
28180844081808441CCA22GENIChomozygous58907431
28180845181808452T-20GENIChomozygous58907432
28180957781809578T-12GENICpossibly homozygous58907433
28180967981809680AATG4GENIChomozygous58907434
28181001781810018GA29GENIChomozygous58907435
28181114081811146ATACAC------3GENIChomozygous58907436
28181125181811252AG7GENIChomozygous58907438
28181364581813646GA23GENIChomozygous58907439
28181368681813687A-6GENIChomozygous58907440
28181412381814124TTC14GENIChomozygous58907441
28181507581815076GA21GENIChomozygous58907442
28181526181815262AG19GENIChomozygous58907443
28181547481815475TC18GENIChomozygous58907444
28181613781816138GA32GENIChomozygous58907445
28181620381816204GA15GENIChomozygous58907446
28181642481816425CT18GENIChomozygous58907447
28181643181816432GA20GENIChomozygous58907448
28181646481816465GA22GENIChomozygous58907449
28181650481816505CT26GENIChomozygous58907450
28181651981816520CT27GENIChomozygous58907451
28181780581817806AG12GENIChomozygous58907452
28181818481818185CT16GENIChomozygous58907454
28182091281820913TTGAG20GENIChomozygous58907456
28182109681821097CG15GENIChomozygous58907457
28181143681811437C-2GENIChomozygous60486684
28181224381812244CCGTGTGTGTGT6GENIChomozygous60486685
28181796481817965TTTGTG2GENIChomozygous60486687