chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166999479166999480TC39GENIChomozygous108357376
1166999495166999496CT39GENIChomozygous108357377
1167000311167000312AG37GENIChomozygous108357378
1167000479167000480GA34GENIChomozygous108357379
1167002035167002036CT47GENIChomozygous108955366
1167002745167002746TA37GENIChomozygous108357382
1167003774167003775GA46GENICpossibly homozygous108955367
1167004661167004662AG23GENIChomozygous108955370
1167004720167004721TC31GENIChomozygous108955371
1167004873167004874AG22GENIChomozygous108955372
1167004963167004964TA24GENICpossibly homozygous108357384
1167005047167005048TC18GENIChomozygous108955373
1167005068167005069GA24GENIChomozygous108955374
1167005076167005077CG23GENIChomozygous108955375
1167007384167007385TC37GENIChomozygous108955378
1167007763167007764AC31GENIChomozygous108357389
1167007845167007846TC41GENIChomozygous108955379
1167009316167009317CT36GENIChomozygous108357390
1167009532167009533TC30GENIChomozygous108357391
1167009857167009858TC30GENIChomozygous108357392
1167011313167011314AG35GENIChomozygous108357396
1167011419167011420AG34GENIChomozygous108357397
1167011457167011458AG27GENIChomozygous108357398
1167011853167011854CT32GENIChomozygous108955386
1167011955167011956TG29GENIChomozygous108357399
1167013919167013920CT36GENICpossibly homozygous109522789