chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84094471540944716G-65GENICheterozygous701101142
84094483540944836C-67GENICheterozygous701101143
84094537740945378TTG88GENICheterozygous701101144
84094773140947732C-77GENICheterozygous701101145
84094826440948265T-77GENICheterozygous701101146
84095043640950437A-27GENICheterozygous701101147
84095794940957950GGCTT6GENICheterozygous701101148
84095844140958442T-25GENICheterozygous701101149
84095852440958525C-8GENICheterozygous701101150
84096328240963283T-9GENIChomozygous701101151
84096347740963478CCT16GENICheterozygous701101152
84096380540963806CCTTT6GENIChomozygous701101155
84096629840966301CTT---43GENICheterozygous701101156
84096840440968405A-17GENIChomozygous701101157
84096998540969986G-111GENICheterozygous701101158
84097026040970261GGCAAGGA3GENICheterozygous701101159
84097608440976085T-72GENICheterozygous701101160
84097616940976170TTA47GENICheterozygous701101161
84098080840980809CCAT35GENICheterozygous701101162
84098087240980873TTC7GENICpossibly homozygous701101163
84098213240982136TGAT----41GENICheterozygous701101164
84098246840982471AAC---31GENICheterozygous701101165