chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT56GENIChomozygous135505436
11286211012862111AG33GENIChomozygous135505437
11286224612862247TC45GENIChomozygous135505438
11286231612862317TC47GENIChomozygous135505439
11286274412862745GT41GENIChomozygous135505440
11286355912863560TG43GENIChomozygous135505441
11286364212863643TA36GENIChomozygous135505442
11286367612863677CT28GENIChomozygous135505443
11286375312863753GTGTGC14GENIChomozygous135395484
11286363712863641GTGC35GENIChomozygous135395481
11286366512863667GC33GENIChomozygous135395482
11286372912863729GTGT18GENIChomozygous135395483
11286379712863799GC5GENIChomozygous135395485
11286381512863817GC8GENIChomozygous135395486
11286382312863829GTGTGT10GENIChomozygous135395487
11286384112863843GC12GENIChomozygous135395488
11286384412863845CT13GENIChomozygous135505444
11286411612864117GC41GENIChomozygous135505445
11286621612866217GA47GENIChomozygous135505446
11286722812867229AG45GENIChomozygous135505447
11286723112867232AG44GENIChomozygous135505448
11286788312867884TC52GENIChomozygous135505449
11286801812868019AC56GENIChomozygous135505450
11286873212868732AAAT34GENICpossibly homozygous135395489
11286876512868767GT37GENIChomozygous135395490
11286899912869000G17GENIChomozygous135395491
11286900312869009TGTGTA17GENIChomozygous135395492
11286901812869024TGGTGT15GENIChomozygous135395493
11286907012869072GT14GENICheterozygous147333387
11286962312869624AG48GENIChomozygous135505451
11287030512870306AG55GENIChomozygous135505452
11287144212871443TC58GENIChomozygous135505453
11287245512872456TA57GENIChomozygous135505454