chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728373617283737GA12GENIChomozygous998314162
141728481617284817CT26GENIChomozygous998314163
141728505217285053TA25GENIChomozygous998314164
141728505817285059CT25GENIChomozygous998314165
141728520317285204GC16GENIChomozygous998314166
141728587617285877CG22GENIChomozygous998314167
141728588117285882CT22GENIChomozygous998314168
141728604017286041GA20GENIChomozygous998314169
141728610817286109AC17GENIChomozygous998314170
141728669517286696CT22GENIChomozygous998314171
141728676817286769TA27GENIChomozygous998314172
141728677617286777TC27GENIChomozygous998314173
141728685817286859TC20GENIChomozygous998314174
141728703617287037CA8GENIChomozygous998314175
141728710317287104CT8GENIChomozygous998314176
141728781917287820TG25GENIChomozygous998314177
141728792417287925CT26GENIChomozygous998314178
141728817517288176GA25GENIChomozygous998314179
141728961817289619GA21GENIChomozygous998314180
141728963217289633AG22GENIChomozygous998314181
141728977417289775GA12GENIChomozygous998314182
141728978717289788AG16GENIChomozygous998314183
141729025017290251TC21GENIChomozygous998314184
141729122717291228CA20GENIChomozygous998314185
141729125217291253TC24GENIChomozygous998314186
141729141717291418CG20GENIChomozygous998314187
141729148217291483GC29GENIChomozygous998314188
141729170017291701CT25GENIChomozygous998314189
141729201917292020CT24GENIChomozygous998314190
141729228617292287GC25GENIChomozygous998314191
141729231617292317CT33GENIChomozygous998314192
141729294717292948GT25GENIChomozygous998314193
141729295017292951CT29GENIChomozygous998314194
141729329117293292TC35GENIChomozygous998314195
141729339117293392AG24GENIChomozygous998314196
141729348817293489AG22GENIChomozygous998314197
141729502417295025TC33GENIChomozygous998314198
141729696617296967GA24GENIChomozygous998314199