chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2236415622236415623GA41GENIChomozygous120327034
2236415949236415950AG21GENIChomozygous110319416
2236416328236416329TC58GENIChomozygous110319420
2236417046236417047GA37GENIChomozygous120397705
2236417786236417787TC63GENIChomozygous110319428
2236420199236420200CT61GENIChomozygous120397706
2236421368236421369TC60GENIChomozygous110319440
2236421808236421809GA54GENIChomozygous120397708
2236422076236422077TC72GENICheterozygous121611587
2236422145236422146AG68GENICheterozygous110319446
2236422159236422160CT64GENICheterozygous111178817
2236422164236422164A66GENICheterozygous135152597
2236423697236423698TC40GENIChomozygous125768882
2236423768236423769TC28GENIChomozygous134927600
2236423748236423749GA34GENIChomozygous134927597
2236423749236423750CA34GENIChomozygous134927598
2236423754236423755AC32GENIChomozygous134927599
2236428657236428658A28GENIChomozygous127751156
2236428676236428677T35GENIChomozygous127751157
2236428762236428763C22GENICpossibly homozygous127751158
2236428772236428773A21GENIChomozygous127751159
2236428783236428783C17GENIChomozygous127751160
2236428798236428798C18GENIChomozygous127751161
2236428814236428815TC16GENIChomozygous110630925
2236428819236428820T15GENIChomozygous127751162
2236428838236428838C8GENIChomozygous127751163
2236428842236428842C8GENIChomozygous127751164
2236428867236428867CC5GENIChomozygous127751165
2236428874236428874T4GENIChomozygous127751166
2236429889236429890CT66GENIChomozygous110319493
2236431383236431384GT52GENIChomozygous120397710
2236431525236431526TA71GENIChomozygous120397712
2236431564236431565GC74GENIChomozygous120397714
2236423889236423890GA32GENICheterozygous133611980