chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160391438160391439TC22GENICpossibly homozygous57763451
3160391483160391484GGT3GENIChomozygous57763452
3160392031160392032AATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT2GENIChomozygous58630001
3160393999160394000TC19GENIChomozygous57763460
3160394215160394216GA33GENICpossibly homozygous57763461
3160394804160394805GC16GENICpossibly homozygous57763462
3160394949160394950GA9GENICpossibly homozygous57763463
3160394995160394996AG15GENICpossibly homozygous57763464
3160395427160395428CT23GENIChomozygous57763465
3160395641160395642AAT3GENICheterozygous57763466
3160395866160395867CT21GENIChomozygous57763469
3160396327160396333CAGAGA------1GENIChomozygous57763474
3160396404160396414AGACAGTGAG----------3GENIChomozygous57763475
3160396457160396458GA8GENICpossibly homozygous57763476
3160396531160396532GA11GENICheterozygous57763479
3160396598160396599GA16GENIChomozygous57763480
3160396756160396757CT11GENICheterozygous57763481
3160396831160396832AG18GENIChomozygous57763482
3160397122160397123AG20GENICheterozygous57763483
3160397274160397275CT8GENIChomozygous57763484
3160397419160397420GA18GENICpossibly homozygous57763485
3160397596160397597AG24GENIChomozygous57763486
3160397724160397725TG29GENIChomozygous57763487
3160397896160397897GA17GENICpossibly homozygous57763488
3160397957160397958AG11GENICpossibly homozygous57763489
3160398285160398286CA19GENICheterozygous57763490
3160398876160398877TC11GENIChomozygous57763491
3160399261160399262AG13GENICpossibly homozygous57763492
3160399521160399522AC14GENICpossibly homozygous57763493
3160399569160399570AC9GENICpossibly homozygous57763494