chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34098575640985757AT24GENIChomozygous112337813
34098633140986332CT31GENIChomozygous112337814
34098735840987359AG15GENIChomozygous111550125
34098739640987397TC15GENIChomozygous111550126
34098793240987933GT30GENIChomozygous111550127
34098798840987989GA33GENICpossibly homozygous112337815
34099068740990688AG15GENIChomozygous111550129
34099177740991778AG12GENIChomozygous111550136
34099191640991917AC13GENIChomozygous111550138
34099206040992061CT9GENIChomozygous112337816
34099376740993768TG7GENIChomozygous112337817
34099382940993830GA6GENICheterozygous112337818
34099393340993934AT13GENIChomozygous112337819
34099411840994119CT6GENICheterozygous111550146
34099741840997419GT8GENIChomozygous112337820
34099745540997456CT12GENIChomozygous112337821
34099971940999720TC12GENIChomozygous111550147
34100043641000437GA16GENIChomozygous112337822
34100061741000618CT19GENIChomozygous111550149
34100101541001016CT8GENIChomozygous112337823
34100168641001687AT9GENIChomozygous112337824
34100205541002056TC12GENIChomozygous111550150
34100402641004027TC4GENIChomozygous111550152
34100412341004124CT5GENIChomozygous111550153
34100434041004341GT7GENIChomozygous111550154
34100463241004633TC8GENIChomozygous111550155
34100664941006650AG16GENIChomozygous111550157
34100785841007859GT8GENIChomozygous111550158
34101007241010073CT16GENIChomozygous111550160
34101116941011170AT13GENIChomozygous111550162
34101170341011704AT19GENIChomozygous111550163
34101181941011820TC6GENICheterozygous111550164
34101207841012079GA10GENIChomozygous111550165
34101211741012118GC13GENIChomozygous111550166
34101249541012496TC17GENIChomozygous111550167
34101257641012577TC45GENIChomozygous111550168
34101310841013109AG32GENIChomozygous111550169
34101335241013353AG14GENICpossibly homozygous111550170
34101510441015105CG24GENIChomozygous111550171
34101635341016354CT17GENICpossibly homozygous112337825
34101949241019493AC14GENIChomozygous111550173
34101976441019765CT16GENIChomozygous111550174