chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106421084664210847AG5GENIChomozygous51904408
106421086264210863GA5GENIChomozygous51904410
106421226464212265GA14GENIChomozygous51904412
106421269964212700G-16GENICpossibly homozygous51476215
106421549864215499CCA10GENIChomozygous51904416
106421580464215805CA27GENIChomozygous51904418
106421595464215955AG24GENIChomozygous51904420
106421617964216180AAAAAC14GENIChomozygous51904422
106421648264216483CCA4GENICheterozygous51476218
106421722064217221GA27GENIChomozygous51476220
106421727364217276AAA---13GENICheterozygous51673982
106422019964220200A-10GENIChomozygous51904424
106422038864220389CT31GENIChomozygous51904426
106422050964220510TA52GENIChomozygous51904428
106422091364220915AC--49GENIChomozygous51904430
106422117064221172CA--41GENIChomozygous51673988
106422120664221207GC41GENIChomozygous51904432
106422229764222298GA25GENIChomozygous51904434
106422316964223170AG12GENIChomozygous51904436
106422679364226794GT28GENIChomozygous51476225
106421727564217276A-13GENICheterozygous52381483
106422361464223620GTGTGT------2GENIChomozygous52381487