chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
195463421554634216GGTCCTTGTCC1GENIChomozygous46410348
195463422654634227CCCTT1GENIChomozygous46410350
195463424154634242CCCTCCCT1GENIChomozygous46410352
195463439254634393TTG9GENIChomozygous46165145
195463448554634486GA1GENIChomozygous46165149
195463449254634493CA1GENIChomozygous46165150
195463462454634625T-1GENIChomozygous46165151
195463463554634636GGATTTATTC1GENIChomozygous46165152
195463474954634750GA3GENIChomozygous46165154
195463529454635295CCAT18GENIChomozygous46165155
195463548254635500ATACACACACACACACAC------------------7GENIChomozygous46566973
195463829854638299GA17GENIChomozygous46165156
195463868754638692CGGGA-----1GENIChomozygous46410360
195463873454638735TTCCAGATGTGGCTTTACAGCCGGGGCAGTACCTTGGGC6GENIChomozygous46410362
195463509054635091CT12GENIChomozygous46296750
195464192354641924GGAA2GENIChomozygous46263176
195464211254642113CCAAAAAAA13GENIChomozygous46410364
195464314654643147CG20GENIChomozygous46165160
195464328054643281CT16GENIChomozygous46165161
195464388854643889CT26GENIChomozygous46165162
195464424554644246GT16GENIChomozygous46165163
195464558754645588GA10GENIChomozygous46165164
195464837354648374GGA9GENIChomozygous46165165
195464998754649988AAG13GENIChomozygous46165166
195465008754650088GC16GENIChomozygous46165168
195465009154650092TC16GENIChomozygous46165169
195465060054650601CT23GENIChomozygous46165170
195465140454651405GA20GENIChomozygous46165171
195465197954651980CCT8GENICheterozygous46165172
195465197954651980CCTT8GENICheterozygous46165173
195465311954653120TC26GENIChomozygous46165180
195465391054653911AG20GENIChomozygous46165183
195465445354654454GA17GENIChomozygous46263186
195465515954655160GT17GENIChomozygous46263187
195465526954655270CT13GENIChomozygous46165184
195465551854655519CCTG5GENICheterozygous46165185
195465551854655519CCTGTG5GENICheterozygous46165186
195465582754655849GAGAGAGAGCGAGAGAGCGAGC----------------------5GENICheterozygous46410368