chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1137126853137126854AC19GENIChomozygous108243360
1137126963137126964CT38GENIChomozygous108243362
1137127022137127023TG37GENIChomozygous108243364
1137128509137128510CT12GENICheterozygous108243371
1137128827137128828AG15GENIChomozygous108243373
1137129176137129177TG11GENIChomozygous108243377
1137136358137136359GA59GENICheterozygous108743232
1137136359137136360GA59GENICheterozygous109141856
1137136362137136363TA59GENICheterozygous108243393
1137136383137136384AG57GENICheterozygous109141862
1137136394137136395GC62GENICheterozygous108743233
1137136440137136441CA62GENICheterozygous109141864
1137136467137136468AC60GENICheterozygous109141866
1137136470137136471GC62GENICheterozygous109141868
1137141106137141107GC21GENIChomozygous108243405
1137168090137168091TG31GENIChomozygous108243458
1137171305137171306CT31GENICheterozygous108243466
1137238936137238937CT6GENIChomozygous108243594
1137238951137238952TG3GENIChomozygous108743240
1137238955137238956TG2GENIChomozygous109326310
1137238957137238958TG2GENIChomozygous109326311
1137238959137238960TA2GENIChomozygous109326312