chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81636153016361531CG14GENIChomozygous52925051
81636154916361550CCCGGA16GENICpossibly homozygous52529138
81636155416361555GC18GENICpossibly homozygous52529140
81636156516361566AAG21GENIChomozygous52529142
81636158516361586GGC18GENICheterozygous52529144
81636158716361588GGCT18GENICheterozygous52529146
81636165116361652G-9GENICheterozygous52529154
81636172316361726GGG---10GENICpossibly homozygous52529156
81636176016361761CCGACCTGGA5GENICheterozygous52529158
81640722816407229TTC23GENICheterozygous53357290
81640972916409730G-4GENICheterozygous53549866
81640973316409734TTA4GENICheterozygous53549867
81640973616409737TTA4GENICheterozygous53549868
81641040916410410TTGTAG53GENICheterozygous53373582
81640740116407403GG--11GENICheterozygous53373578
81640747116407480GTTTTTTTT---------5GENICheterozygous53373579
81641061416410615T-30GENICheterozygous52529207
81641143916411444AAGGC-----1GENIChomozygous53549869