chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1156283132156283133CT50GENIChomozygous108322223
1156283581156283583TA51GENIChomozygous127448632
1156284687156284688CT52GENIChomozygous108322225
1156285112156285113GC47GENIChomozygous108322227
1156285132156285133CA46GENIChomozygous108322229
1156285153156285154G31GENICheterozygous127448633
1156285417156285418TC52GENIChomozygous108322231
1156285463156285464AG56GENIChomozygous108322233
1156285477156285477ATTTAAGAAGCAT51GENIChomozygous127448634
1156285893156285894GC58GENIChomozygous108322235
1156286459156286460TC39GENIChomozygous108322237
1156286801156286802GA50GENIChomozygous108322239
1156287003156287004AG58GENIChomozygous108322241
1156287482156287483AT74GENIChomozygous108322243
1156288291156288292T38GENIChomozygous127448635
1156288416156288417AG53GENIChomozygous108322245
1156285174156285175AC41GENIChomozygous108750037
1156289245156289246CT58GENIChomozygous108322247
1156289709156289710TC53GENIChomozygous108322249
1156289864156289865TC59GENIChomozygous108322251
1156290057156290058CT42GENIChomozygous108322253
1156290558156290559TA62GENIChomozygous108322255
1156291001156291005TAAC56GENIChomozygous127448636
1156291017156291018GA53GENIChomozygous108322257