chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1148242763148242764TC15GENICheterozygous108288021
1148242838148242839AG17GENICheterozygous108288023
1148242920148242921CT14GENICheterozygous108288025
1148243024148243025CT11GENICheterozygous108288029
1148243029148243030AG12GENICheterozygous108288031
1148243031148243032CT12GENICheterozygous108288033
1148243035148243036GT12GENICheterozygous108288035
1148265855148265856CA6GENICheterozygous120486630
1148265856148265857AT6GENICheterozygous120486631
1148265874148265875TG7GENICheterozygous109331500
1148265888148265889GA8GENICheterozygous109331502
1148265921148265922CA6GENICheterozygous109331504
1148265933148265934GA2GENIChomozygous109331506
1148266404148266405TC8GENICheterozygous109331525
1148266417148266418CT10GENICheterozygous109331527
1148266427148266428GC8GENICpossibly homozygous109331529
1148266465148266466CT9GENICheterozygous109331531
1148266686148266687GT6GENICheterozygous109331537
1148266701148266702TA6GENICheterozygous109331539
1148266710148266711TG5GENICheterozygous109331541
1148266741148266742CT4GENICheterozygous109331543
1148266748148266749AG5GENICheterozygous109331545
1148285561148285562TC7GENICpossibly homozygous109331671