chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28695978386959784TC43GENIChomozygous136204143
28696019386960194AG39GENIChomozygous141396531
28696170786961708GC45GENIChomozygous136204153
28696171386961714AG45GENIChomozygous136204154
28696205386962054GA30GENIChomozygous136204155
28696220486962205TC30GENIChomozygous136204156
28696220586962206GT30GENIChomozygous136204157
28696253686962537C18GENIChomozygous135924953
28696253886962551GGGGTGGGGGGTC18GENIChomozygous135924954
28696273186962732AC46GENIChomozygous136204158
28696371686963717AT37GENIChomozygous136204160
28696379986963800CG42GENIChomozygous136204161
28696389486963895TC48GENIChomozygous136204162
28696405786964058AC46GENIChomozygous144303287
28696225786962258AG37GENIChomozygous144303284
28696348086963481GA44GENIChomozygous144303285
28696348586963486GA45GENIChomozygous144303286
28696407986964080TC43GENIChomozygous136204163
28696426286964263AG39GENIChomozygous136204164
28696511486965115TC47GENIChomozygous136204166
28696511586965116AG48GENIChomozygous136204167
28696530386965304TC38GENIChomozygous136204168
28696611086966111TC45GENIChomozygous136204170
28696612786966128GA52GENIChomozygous144303288
28696674086966741TC52GENICpossibly homozygous136204172
28696728086967281TA50GENIChomozygous136204173
28696728286967283TG49GENIChomozygous136204174
28696255086962551C18GENIChomozygous403011131
28696255086962551CG18GENICheterozygous403011132