chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170621711170621712GGA8GENIChomozygous61909297
1170622756170622757TC7GENIChomozygous60941111
1170623122170623123CA7GENIChomozygous60941112
1170623281170623282TC13GENIChomozygous61909298
1170623994170623995GC2GENIChomozygous61909299
1170624733170624734CT5GENIChomozygous61909300
1170625101170625102GA6GENIChomozygous61909301
1170625345170625346GA10GENIChomozygous61909302
1170626576170626580TAAA----5GENIChomozygous61909303
1170626744170626745AAAC5GENICheterozygous62271169
1170626744170626745AAACAC5GENICheterozygous62544949
1170628280170628281GA11GENIChomozygous61909304
1170628709170628710AG14GENIChomozygous60941115
1170629075170629076GGAA13GENICheterozygous60941116
1170629075170629076GGA13GENICheterozygous62313534
1170629076170629077A-13GENICheterozygous61909305
1170629637170629638GA7GENIChomozygous60941117
1170631272170631273GA4GENIChomozygous61909306
1170631445170631446TC6GENIChomozygous60941118
1170631481170631482CA10GENIChomozygous62579978
1170632202170632203TC5GENIChomozygous60941121
1170632326170632327CT11GENIChomozygous61909307
1170632351170632352GA11GENIChomozygous61909308