chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897652078976521AC27GENIChomozygous108873367
17897652978976530CT25GENIChomozygous108873368
17897686378976864GA26GENIChomozygous108873369
17897704278977043GC17GENIChomozygous108873370
17897712078977121CT23GENIChomozygous108873371
17897762678977627TC26GENIChomozygous108873372
17897818278978183CT78GENICpossibly homozygous108873373
17897889978978900CT27GENIChomozygous108873375
17897920778979208TA23GENIChomozygous108873376
17897927378979274CT19GENIChomozygous108873377
17897934178979342GA18GENIChomozygous108873378
17897938978979390CT19GENIChomozygous108873379
17897966278979663CT32GENIChomozygous108873380
17898319378983194GA24GENICpossibly homozygous108873384
17898330978983310AT21GENIChomozygous108873385
17898381078983811TC30GENIChomozygous108873386
17898739078987391GA32GENIChomozygous108873390
17898773078987731AC15GENIChomozygous108873392
17898947678989477GA42GENIChomozygous108873396
17898995778989958TC21GENIChomozygous108873397
17899010278990103AG29GENIChomozygous108873398
17899081078990811CT18GENIChomozygous108873400
17899097878990979TC24GENIChomozygous108873401
17899258778992588AG23GENIChomozygous108873406
17899274978992750TC30GENIChomozygous108873407
17899300878993009TC23GENIChomozygous108873408
17899385278993853CT16GENIChomozygous108873409
17899446978994470CT24GENIChomozygous108873410
17899461278994613GA12GENIChomozygous108873411
17899562578995626CT25GENIChomozygous108873412
17899567078995671AT30GENIChomozygous108873413
17899595378995954CT23GENIChomozygous108873414
17899644878996449TG16GENIChomozygous108873415