chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148160147481601475TC15GENIChomozygous623468893
148160185981601860TA10GENIChomozygous623468894
148160188881601889AG14GENIChomozygous623468895
148160192281601923GA16GENIChomozygous623468896
148160194181601942TC12GENIChomozygous623468897
148160231181602312TC19GENIChomozygous623468898
148160247181602474CTC---7GENICpossibly homozygous740247751
148160278981602790AG4GENIChomozygous623468899
148160282181602822AG8GENICpossibly homozygous623468900
148160288081602890GGCCGCAGAG----------3GENICheterozygous740247752
148160299981603000AG12GENICpossibly homozygous623468901
148160318481603185GA17GENIChomozygous623468902
148160353981603540CT11GENIChomozygous623468903
148160362381603624GA12GENICpossibly homozygous623468904
148160386581603866CCCT3GENIChomozygous740247753
148160386881603869TC3GENIChomozygous623468905
148160416381604164CG8GENICpossibly homozygous623468906
148160437181604372GT28GENIChomozygous623468907
148160462781604628AG19GENICpossibly homozygous623468908
148160469281604693AC18GENICpossibly homozygous623468909
148160470481604705CT19GENICpossibly homozygous623468910
148160486881604869GA16GENICpossibly homozygous623468911
148160489481604895GA11GENIChomozygous623468912
148160514481605145CG14GENIChomozygous623468913
148160569981605700TG14GENICheterozygous623468914
148160607181606072TG5GENICheterozygous623468915
148160611781606118GT2GENICheterozygous623468916
148160691181606912TC15GENICpossibly homozygous623468917
148160694681606947CT10GENICheterozygous623468918
148160920981609210CT14GENICpossibly homozygous623468919
148160970281609703GA11GENICpossibly homozygous623468920
148160972681609727TG9GENIChomozygous623468921
148161055381610554TC4GENICheterozygous623468922