chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2135092952135092953GA25GENIChomozygous59095165
2135094312135094313C-17GENICpossibly homozygous59095167
2135094724135094725GA20GENIChomozygous59095169
2135094770135094771AG17GENIChomozygous59095171
2135095106135095107GA15GENIChomozygous59095173
2135095565135095566AAT5GENIChomozygous59095175
2135095741135095742A-3GENICheterozygous60498524
2135097000135097001GA12GENIChomozygous59095177
2135097154135097155TC2GENIChomozygous59095179
2135097869135097870CT10GENIChomozygous59095181
2135098269135098270AT21GENICheterozygous59095183
2135098663135098664GGAACTATTAACTTATAACTGTGAACTTAT1GENIChomozygous59095185
2135099175135099176GA13GENIChomozygous59095187
2135099272135099273GA16GENIChomozygous59095189
2135099301135099302AG25GENIChomozygous59095191
2135099841135099842TC15GENICheterozygous59095193
2135099867135099868CG9GENICpossibly homozygous59095195
2135100318135100322TATA----7GENICheterozygous59095197
2135100498135100500CT--4GENICheterozygous59095199
2135104674135104675TG7GENICpossibly homozygous60450530
2135107243135107244AG14GENIChomozygous59760378
2135107244135107245GT13GENIChomozygous59760379
2135107299135107300CT14GENIChomozygous59095216
2135108250135108251CT20GENICpossibly homozygous59095218
2135108297135108299TT--7GENIChomozygous59095220
2135108556135108557AG14GENIChomozygous59095222
2135109020135109021TG13GENICheterozygous59095224
2135109221135109222CA20GENICpossibly homozygous59095226
2135109242135109243CT18GENICpossibly homozygous59095228
2135109338135109339GC6GENICheterozygous59095230
2135109351135109353TG--12GENICheterozygous59095232
2135109403135109404GA17GENICheterozygous59095234
2135109784135109785CT21GENICpossibly homozygous59095236
2135110001135110002AG20GENIChomozygous59095238