chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170621711170621712GGA23GENIChomozygous61909297
1170622756170622757TC15GENIChomozygous60941111
1170623122170623123CA26GENIChomozygous60941112
1170623281170623282TC28GENIChomozygous61909298
1170623994170623995GC14GENIChomozygous61909299
1170624336170624337TTCACACACACACA5GENIChomozygous62173309
1170624733170624734CT9GENIChomozygous61909300
1170625101170625102GA15GENIChomozygous61909301
1170625345170625346GA33GENIChomozygous61909302
1170626576170626580TAAA----15GENIChomozygous61909303
1170626744170626745AAACAC3GENIChomozygous62544949
1170628280170628281GA12GENIChomozygous61909304
1170628709170628710AG22GENIChomozygous60941115
1170629075170629076GGAA7GENICheterozygous60941116
1170629637170629638GA18GENIChomozygous60941117
1170631272170631273GA13GENIChomozygous61909306
1170631445170631446TC16GENIChomozygous60941118
1170632202170632203TC19GENIChomozygous60941121
1170632326170632327CT20GENIChomozygous61909307
1170632351170632352GA25GENIChomozygous61909308
1170631481170631482CA11GENICpossibly homozygous62579978