chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186702772186702773TC59GENIChomozygous110166426
2186702922186702923CT53GENICpossibly homozygous110166427
2186704010186704011TC30GENIChomozygous110166428
2186704176186704177TC4GENIChomozygous110166429
2186704186186704187TG26GENIChomozygous110166430
2186704218186704219GT45GENICpossibly homozygous110166431
2186704227186704228GA49GENICpossibly homozygous110166432
2186704244186704245GT37GENIChomozygous110166433
2186704246186704247GC37GENIChomozygous110166434
2186704253186704254AC37GENIChomozygous110166435
2186704798186704799CA47GENIChomozygous110166436
2186712730186712731TC45GENIChomozygous110166437
2186714882186714883AG36GENIChomozygous110166438
2186715666186715667TG61GENIChomozygous110166439
2186716227186716228AG54GENIChomozygous110166440
2186718012186718013AT25GENICpossibly homozygous110166441
2186718964186718965TC48GENICpossibly homozygous110166442
2186719031186719032AG21GENICpossibly homozygous110166443
2186719343186719344TC104GENICheterozygous110166445
2186719361186719362TA78GENICheterozygous110166446
2186719649186719650CT63GENIChomozygous110166447
2186719815186719816CG43GENIChomozygous110166448
2186719921186719922GA43GENIChomozygous110166449
2186720026186720027CT28GENIChomozygous110166450
2186720082186720083GA53GENIChomozygous110166451
2186720993186720994TG47GENIChomozygous110166452
2186721071186721072CT37GENIChomozygous110166453
2186721251186721252GA42GENICheterozygous110166454
2186721886186721887TC45GENIChomozygous110166455
2186721894186721895CT46GENIChomozygous110166456
2186722027186722028TG47GENIChomozygous110166457
2186722555186722556GA57GENIChomozygous110166458
2186722559186722560CT51GENIChomozygous110166459
2186711273186711274GA183GENICheterozygous110614105