chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2135092952135092953GA17GENICpossibly homozygous59095165
2135094312135094313C-23GENIChomozygous59095167
2135094724135094725GA28GENIChomozygous59095169
2135094770135094771AG33GENIChomozygous59095171
2135095106135095107GA19GENIChomozygous59095173
2135095565135095566AAT24GENIChomozygous59095175
2135095741135095743AA--15GENICheterozygous59760376
2135095742135095743A-15GENICheterozygous59760377
2135097000135097001GA17GENICpossibly homozygous59095177
2135097154135097155TC6GENIChomozygous59095179
2135097869135097870CT19GENIChomozygous59095181
2135098269135098270AT20GENIChomozygous59095183
2135098663135098664GGAACTATTAACTTATAACTGTGAACTTAT7GENIChomozygous59095185
2135099175135099176GA24GENIChomozygous59095187
2135099272135099273GA22GENIChomozygous59095189
2135099301135099302AG25GENICpossibly homozygous59095191
2135099841135099842TC20GENIChomozygous59095193
2135099867135099868CG22GENIChomozygous59095195
2135100318135100322TATA----15GENIChomozygous59095197
2135100498135100500CT--5GENIChomozygous59095199
2135103954135103968ACACACACACACAC--------------5GENICheterozygous59095207
2135103956135103968ACACACACACAC------------5GENICheterozygous59095209
2135104849135104851TG--24GENICheterozygous59095211
2135105003135105005TG--1GENIChomozygous60055069
2135105746135105747CCTA18GENICpossibly homozygous59095213
2135105747135105748CT19GENICheterozygous59095214
2135107299135107300CT24GENIChomozygous59095216
2135108250135108251CT16GENIChomozygous59095218
2135108297135108299TT--16GENIChomozygous59095220
2135108556135108557AG22GENIChomozygous59095222
2135109020135109021TG29GENIChomozygous59095224
2135109221135109222CA32GENIChomozygous59095226
2135109242135109243CT28GENIChomozygous59095228
2135109338135109339GC15GENIChomozygous59095230
2135109351135109353TG--19GENIChomozygous59095232
2135109403135109404GA27GENIChomozygous59095234
2135109784135109785CT21GENIChomozygous59095236
2135110001135110002AG21GENIChomozygous59095238