chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104293319442933195TC24GENIChomozygous116577058
104293366642933667GC18GENIChomozygous116577062
104293377942933780AG14GENIChomozygous116577064
104293440442934405AG28GENIChomozygous116577066
104293447242934473TC20GENIChomozygous116577068
104293456142934562GA21GENIChomozygous116577072
104293471542934716CA16GENIChomozygous116577074
104293472742934728CT17GENIChomozygous116930403
104293480342934804TC24GENIChomozygous116577076
104293591742935918AG23GENIChomozygous116577078
104293644042936441TA19GENIChomozygous116930405
104293652342936524TC20GENIChomozygous116577084
104293665342936654CG26GENIChomozygous116930407
104293681242936813AG26GENIChomozygous116577088
104293750942937510AG19GENIChomozygous116577090
104293759742937598TG34GENIChomozygous116577094
104293875542938756GA18GENIChomozygous116930409
104293877242938773AG19GENIChomozygous116930411
104294020842940209AC14GENIChomozygous116930413
104294084142940842GA22GENIChomozygous116930415
104294154042941541GA5GENIChomozygous116930417
104294196142941962GA20GENIChomozygous116577142
104294317042943171GA8GENIChomozygous116930419
104294330642943307AT19GENIChomozygous116577150
104294352842943529GA22GENIChomozygous116577152
104294371042943711GA10GENIChomozygous116930421
104294526442945265CT27GENIChomozygous116577156