chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101368583101368584TC21GENIChomozygous783563884
1101368760101368761AT17GENIChomozygous783563885
1101369073101369074AG20GENIChomozygous783563886
1101370389101370390GA16GENIChomozygous783563887
1101370673101370674TC21GENIChomozygous783563888
1101370736101370737AT23GENIChomozygous783563889
1101370770101370771CT24GENIChomozygous783563890
1101371580101371581GC22GENIChomozygous783563891
1101372581101372582TC22GENIChomozygous783563892
1101376054101376055CT21GENIChomozygous783563893
1101376215101376216AG17GENIChomozygous783563894
1101376401101376402TG23GENIChomozygous783563895
1101376696101376697TC16GENIChomozygous783563896
1101376846101376847AT15GENIChomozygous783563897
1101376887101376888TA19GENICpossibly homozygous783563898
1101377139101377140GA17GENICpossibly homozygous783563899
1101378208101378209CA16GENIChomozygous783563900
1101380569101380570AG26GENIChomozygous783563901
1101380582101380583CT26GENIChomozygous783563902
1101380673101380674GA27GENIChomozygous783563903
1101381127101381128AG21GENIChomozygous783563904
1101381367101381368CT26GENICpossibly homozygous783563905
1101382022101382023TG28GENIChomozygous783563906
1101383176101383177GA25GENIChomozygous783563907
1101383339101383340TC23GENIChomozygous783563908
1101384591101384592AG19GENICpossibly homozygous783563909
1101385268101385269TC28GENIChomozygous783563910
1101385945101385946CA23GENIChomozygous783563911
1101387193101387194CT22GENIChomozygous783563912