chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X3274708932747090AG8GENIChomozygous108253037
X3275072132750722AG11GENIChomozygous108253045
X3275639632756397TC8GENIChomozygous108253047
X3275747032757471CT9GENIChomozygous108253049
X3276222432762225AG5GENIChomozygous108253053
X3276254232762543CG6GENIChomozygous108253055
X3276317632763177AC9GENIChomozygous108253058
X3276338032763381GA6GENIChomozygous108253060
X3276353432763535CG11GENIChomozygous108253062
X3276354932763550CT12GENIChomozygous108253064
X3276411432764115AG6GENIChomozygous108253066
X3276465232764653GA10GENIChomozygous108253070
X3276476532764766TC8GENIChomozygous108253072
X3276538032765381CA10GENIChomozygous108253074
X3276595532765956AG6GENIChomozygous108253076
X3276772932767730AG5GENIChomozygous108253080
X3276899232768993AC9GENIChomozygous108253084
X3276929632769297TA4GENIChomozygous108253086
X3276933432769335CT7GENIChomozygous108253088
X3276988432769885AC5GENIChomozygous108253090
X3277041432770415AG9GENIChomozygous108253092
X3277051532770516CT9GENIChomozygous108253094
X3277056032770561AG10GENIChomozygous108253096
X3277079132770792CT10GENICheterozygous108253098
X3278118532781186GT6GENIChomozygous108253102
X3278218732782188TC9GENIChomozygous108253104
X3278255132782552AG8GENIChomozygous108253106
X3278307732783078CA7GENIChomozygous119914096
X3278312632783127AG4GENICheterozygous119914098
X3278444032784441GT8GENIChomozygous119914100
X3278572132785722CG6GENIChomozygous108253108
X3278621332786214AT9GENIChomozygous108253110