chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1186858917186858918AG41GENIChomozygous74633249
1186859676186859677CG52GENIChomozygous74633251
1186862369186862370CT62GENIChomozygous74633253
1186862473186862474AC62GENIChomozygous74633255
1186862692186862693CA67GENICpossibly homozygous74633257
1186863917186863918GC27GENIChomozygous75462606
1186864590186864591CG36GENICpossibly homozygous75462608
1186864692186864693AG18GENIChomozygous75462610
1186867171186867172AC53GENICpossibly homozygous74633261
1186867587186867588TC57GENIChomozygous74633262
1186867883186867884CT62GENIChomozygous75462612
1186867963186867964TC55GENIChomozygous75462614
1186867992186867993TC39GENICpossibly homozygous75462616
1186867993186867994GA38GENICpossibly homozygous75462618
1186868500186868501CG38GENIChomozygous75342717
1186868561186868562AG27GENIChomozygous75462620
1186868831186868832GT59GENIChomozygous75462622
1186869124186869125TC18GENICpossibly homozygous75462624
1186869156186869157AG15GENIChomozygous74633270
1186869354186869355AG48GENIChomozygous74633272
1186870514186870515AG40GENIChomozygous74633274