chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148234593148234595AC12GENICheterozygous141089596
4148247084148247085AG19GENIChomozygous141090606
4148247100148247101GA17GENIChomozygous137229020
4148247102148247103AG18GENIChomozygous141090607
4148316243148316244GC5GENICheterozygous403767977
4148247090148247091GA19GENIChomozygous403590120
4148247090148247091G19GENICheterozygous403590121
4148247102148247103A18GENICheterozygous404045644
4148295194148295195G12GENICpossibly homozygous403767974
4148295194148295195GC12GENICheterozygous403767975
4148316243148316244G5GENICheterozygous403767976
4148272485148272485ACAC9GENICpossibly homozygous140995933