chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106421084664210847AG14GENIChomozygous51904408
106421086264210863GA14GENIChomozygous51904410
106421226464212265GA22GENIChomozygous51904412
106421269964212700G-13GENIChomozygous51476215
106421549864215499CCA19GENICheterozygous51904416
106421580464215805CA19GENIChomozygous51904418
106421595464215955AG15GENIChomozygous51904420
106421617964216180AAAAAC5GENIChomozygous51904422
106421648264216483CCAA8GENICheterozygous51476217
106421648264216483CCA8GENICheterozygous51476218
106421722064217221GA9GENIChomozygous51476220
106421727364217276AAA---15GENIChomozygous51673982
106422019964220200A-14GENIChomozygous51904424
106422038864220389CT16GENIChomozygous51904426
106422050964220510TA26GENICpossibly homozygous51904428
106422091364220915AC--15GENICpossibly homozygous51904430
106422117064221172CA--23GENIChomozygous51673988
106422120664221207GC27GENIChomozygous51904432
106422229764222298GA20GENIChomozygous51904434
106422316964223170AG23GENIChomozygous51904436
106422361464223620GTGTGT------1GENIChomozygous52381487
106422679364226794GT18GENIChomozygous51476225