chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1156283132156283133CT53GENIChomozygous108322223
1156283581156283583TA47GENICpossibly homozygous127448632
1156284687156284688CT46GENIChomozygous108322225
1156285112156285113GC41GENIChomozygous108322227
1156285132156285133CA42GENIChomozygous108322229
1156285153156285154G36GENICheterozygous127448633
1156285417156285418TC61GENIChomozygous108322231
1156285463156285464AG66GENIChomozygous108322233
1156285477156285477ATTTAAGAAGCAT60GENIChomozygous127448634
1156285893156285894GC48GENIChomozygous108322235
1156286459156286460TC54GENIChomozygous108322237
1156286801156286802GA48GENICpossibly homozygous108322239
1156287003156287004AG51GENIChomozygous108322241
1156287482156287483AT47GENIChomozygous108322243
1156288291156288292T39GENIChomozygous127448635
1156288416156288417AG55GENIChomozygous108322245
1156285174156285175AC45GENICpossibly homozygous108750037
1156289245156289246CT38GENIChomozygous108322247
1156289709156289710TC55GENIChomozygous108322249
1156289864156289865TC47GENIChomozygous108322251
1156290057156290058CT54GENIChomozygous108322253
1156290558156290559TA40GENIChomozygous108322255
1156291001156291005TAAC45GENIChomozygous127448636
1156291017156291018GA49GENIChomozygous108322257