chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2135092952135092953GA25GENIChomozygous59095165
2135094312135094313C-19GENIChomozygous59095167
2135094724135094725GA10GENIChomozygous59095169
2135094770135094771AG4GENIChomozygous59095171
2135095106135095107GA20GENICpossibly homozygous59095173
2135095565135095566AAT1GENIChomozygous59095175
2135097000135097001GA14GENICpossibly homozygous59095177
2135097154135097155TC3GENIChomozygous59095179
2135097869135097870CT7GENICheterozygous59095181
2135098269135098270AT17GENICpossibly homozygous59095183
2135098663135098664GGAACTATTAACTTATAACTGTGAACTTAT1GENIChomozygous59095185
2135099175135099176GA17GENICpossibly homozygous59095187
2135099272135099273GA20GENICpossibly homozygous59095189
2135099301135099302AG26GENIChomozygous59095191
2135099841135099842TC21GENICpossibly homozygous59095193
2135099867135099868CG9GENICheterozygous59095195
2135100318135100322TATA----7GENICpossibly homozygous59095197
2135100498135100500CT--3GENICheterozygous59095199
2135104674135104675TG11GENICpossibly homozygous60450530
2135107243135107244AG10GENIChomozygous59760378
2135107244135107245GT10GENIChomozygous59760379
2135107299135107300CT19GENICpossibly homozygous59095216
2135108250135108251CT26GENICpossibly homozygous59095218
2135108297135108299TT--9GENIChomozygous59095220
2135108556135108557AG15GENIChomozygous59095222
2135109020135109021TG14GENIChomozygous59095224
2135109221135109222CA16GENICpossibly homozygous59095226
2135109242135109243CT19GENIChomozygous59095228
2135109338135109339GC5GENIChomozygous59095230
2135109351135109353TG--4GENIChomozygous59095232
2135109403135109404GA11GENICheterozygous59095234
2135109784135109785CT15GENIChomozygous59095236
2135110001135110002AG24GENIChomozygous59095238