chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2234378944234378945TG5GENIChomozygous59445905
2234379102234379103TA16GENICpossibly homozygous59445906
2234379126234379127GC10GENIChomozygous59445907
2234379244234379245TC14GENIChomozygous59445909
2234379282234379283AG5GENIChomozygous59445910
2234379386234379388CT--3GENIChomozygous59445911
2234381020234381021CT10GENIChomozygous59445913
2234381568234381580CTTTAGGCCTAC------------1GENIChomozygous60170982
2234381679234381680AAG7GENIChomozygous59445914
2234381752234381753CA9GENIChomozygous59445915
2234382626234382627CT4GENICheterozygous59445917
2234383136234383137T-3GENIChomozygous59445918
2234383428234383429CA7GENIChomozygous59445919
2234385211234385212CT19GENICpossibly homozygous59445923
2234385275234385276AC17GENICpossibly homozygous59445924
2234385429234385430CT13GENICheterozygous59445925
2234385504234385505AC12GENICpossibly homozygous59445926
2234385645234385646CT15GENIChomozygous59445927
2234385769234385770CT10GENIChomozygous60170983
2234385831234385832TTA7GENICheterozygous59445928
2234385831234385832TTAA7GENICheterozygous59942199
2234386497234386498TC15GENIChomozygous59445933
2234386576234386577TC10GENIChomozygous59445934
2234386727234386728TG8GENIChomozygous59445935
2234386758234386759TC13GENIChomozygous59445936
2234386832234386833AAT8GENIChomozygous59445937
2234386869234386870TC13GENICpossibly homozygous59445938
2234387446234387447GA10GENIChomozygous59445939
2234387707234387708GA10GENIChomozygous59445941
2234387975234387976AG18GENICpossibly homozygous59445942