chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
317410741741074T30GENIChomozygous127844010
317550681755068GA44GENIChomozygous127844012
317551021755102G48GENIChomozygous127844013
317552521755252G34GENIChomozygous127844014
317553381755339A3GENIChomozygous130277112
317555061755507TG4GENIChomozygous130285551
317555071755508GT3GENIChomozygous130285552
317459791745980GA21GENICheterozygous127966335
317464151746416GA38GENICheterozygous111868297
317551501755151TG63GENIChomozygous111868299
317466321746633AG21GENICheterozygous111428401
317466591746660TC13GENICheterozygous111428402
317551491755150GT63GENIChomozygous119696967
318065921806593CT18GENIChomozygous111428404
318124421812443GT23GENIChomozygous111428405
318347991834800CG10GENICheterozygous130285553
318348901834890AGAGGCGGGCAGAGGCGGAGAGAGGCGGGCAGAGGCGGAGAGAGGCGGGC10GENICheterozygous127844018
318349441834945TG12GENIChomozygous111428408
318801131880113A32GENICheterozygous132038086
318910581891062ATCA23GENIChomozygous130277116
318980501898051GT7GENIChomozygous111428417
318981291898130GA16GENIChomozygous125805388
319083651908366GT16GENICpossibly homozygous111428430
319159511915952CT52GENIChomozygous134675233