chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4178143100178143101CA5GENICheterozygous112969583
4178150228178150229CT8GENICheterozygous126041449
4178150258178150259TC5GENIChomozygous126041450
4178208794178208795CG18GENIChomozygous126030768
4178208812178208813CG10GENIChomozygous126030769
4178208821178208822CA4GENIChomozygous126041451
4178219905178219906CT15GENIChomozygous126030770
4178261406178261407TA4GENICheterozygous126041452
4178366066178366067CT4GENIChomozygous126041453
4178399868178399869TA3GENICheterozygous126041454
4178659876178659877TC4GENICheterozygous126041455
4178660305178660306CG3GENICheterozygous126041456
4178702034178702035CA14GENIChomozygous126030796
4178702042178702043CA15GENIChomozygous126030797
4178702085178702086CT11GENIChomozygous126030798
4178702148178702149CT5GENIChomozygous126030799
4178728952178728953GA6GENICheterozygous112970451
4178728960178728961GA4GENICheterozygous112970452
4178728966178728967GA6GENICheterozygous112970453
4178844748178844749GA3GENICheterozygous126041457
4178857489178857490AC21GENICheterozygous112970746
4178863399178863400AG11GENIChomozygous112970759
4178863739178863740AC8GENIChomozygous112970765
4178863749178863750TC11GENIChomozygous112970766
4178863815178863816CA12GENIChomozygous112970767
4178863834178863835TA10GENIChomozygous112970768
4178863930178863931GA18GENIChomozygous112970769
4178875330178875331AT11GENIChomozygous126041458
4178900182178900183GC3GENICheterozygous126041459
4178972237178972238CA3GENICheterozygous126041460