chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1129281859129281860T-9GENICheterozygous62246274
1129284219129284220TTC19GENIChomozygous60850910
1129284426129284427CCAA5GENICheterozygous62157370
1129294447129294448C-8GENIChomozygous60850914
1129309633129309634AG10GENIChomozygous60850925
1129309634129309635CA10GENIChomozygous62087446
1129309641129309642AG10GENIChomozygous62087447
1129309648129309649A-11GENIChomozygous60850926
1129319289129319291GT--5GENICheterozygous62231333
1129320755129320756CCAACACCT22GENIChomozygous60850934
1129320962129320963AAC21GENIChomozygous60850935
1129320981129320982AAC21GENIChomozygous60850936
1129320997129320998AAC23GENIChomozygous60850937
1129321017129321018TTC24GENIChomozygous60850938
1129321052129321053CT21GENIChomozygous62087449
1129321053129321054TC21GENIChomozygous62087450
1129328301129328302C-11GENIChomozygous60850945
1129328767129328768A-6GENICheterozygous62231334
1129330644129330645TTA4GENICheterozygous62157372
1129330654129330655GA7GENIChomozygous60850946
1129330671129330678GCCATCG-------8GENICheterozygous62246275
1129334737129334738CCT25GENIChomozygous60850947
1129337018129337019GGTTA21GENIChomozygous60850950
1129350885129350886G-11GENIChomozygous60850952
1129350909129350910GT13GENIChomozygous60850953
1129358070129358071A-7GENICheterozygous62246276
1129366067129366068TTTCTCTCTCTCTCTC6GENICheterozygous62157374
1129375240129375241CCA35GENICheterozygous60850966
1129375279129375280AAT39GENICheterozygous60850967
1129378086129378087TTA11GENIChomozygous60850971
1129378674129378675A-15GENICheterozygous62231336
1129378946129378947TTACAC7GENICheterozygous62157379
1129378947129378949AC--7GENICheterozygous62157381
1129384679129384680GGGGTGTGTGTGT4GENICheterozygous60850973
1129384679129384680GGGGTGTGTGTGTGT4GENICheterozygous61518200