chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170621711170621712GGA25GENIChomozygous61909297
1170622756170622757TC32GENIChomozygous60941111
1170623122170623123CA26GENIChomozygous60941112
1170623281170623282TC22GENIChomozygous61909298
1170623994170623995GC30GENICpossibly homozygous61909299
1170624336170624337TTCACACACACACA13GENIChomozygous62173309
1170624733170624734CT30GENIChomozygous61909300
1170625101170625102GA39GENIChomozygous61909301
1170625345170625346GA41GENIChomozygous61909302
1170626576170626580TAAA----12GENIChomozygous61909303
1170626744170626745AAACAC3GENIChomozygous62544949
1170628280170628281GA26GENIChomozygous61909304
1170628709170628710AG36GENIChomozygous60941115
1170629637170629638GA28GENIChomozygous60941117
1170631272170631273GA22GENIChomozygous61909306
1170631445170631446TC26GENIChomozygous60941118
1170632202170632203TC46GENIChomozygous60941121
1170632326170632327CT34GENICpossibly homozygous61909307
1170632351170632352GA34GENICpossibly homozygous61909308
1170631481170631482CA22GENIChomozygous62579978