chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182296654822966549T-15INTERGENIChomozygous46388677
182297001922970021AA--15INTERGENIChomozygous46650642
182297152522971526CT17INTERGENIChomozygous46650643
182297159922971600CG12INTERGENIChomozygous46650644
182297179022971791AACCAGCTGAACTAGTGGGG14INTERGENIChomozygous46388684
182297183422971835CT20INTERGENIChomozygous46650645
182297184422971845CT21INTERGENIChomozygous46650646
182297212422972125CT26INTERGENIChomozygous46650647
182297252722972528GT31INTERGENIChomozygous46650648
182297262522972626TC23INTERGENIChomozygous46650649
182297271722972718TA19INTERGENIChomozygous46650650
182297273822972739AG20INTERGENIChomozygous46650651
182297278222972783TG24INTERGENIChomozygous46650652
182297315622973157GA17INTERGENIChomozygous46650653
182297384322973844CT12INTERGENIChomozygous46650654
182297387922973880CT19INTERGENIChomozygous46650655
182297400122974002AG23INTERGENIChomozygous46388685
182297428622974287TC20INTERGENIChomozygous46388686
182297462022974621CT22INTERGENIChomozygous46650656
182297469822974699GA24INTERGENIChomozygous46650657
182297504222975043T-18INTERGENIChomozygous46388689
182297576922975770CG15INTERGENIChomozygous46388690
182298848822988489GA25INTERGENIChomozygous46650666
182300683723006838GGT9INTERGENICheterozygous46389014
182300683723006838GGTT9INTERGENICheterozygous46389015
182302602123026022AATCTCT7INTERGENIChomozygous46389098
182303840523038407TG--9INTERGENIChomozygous46811366