chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2082726518272652CG24GENIChomozygous45416637
2082730618273062AC23GENIChomozygous45416639
2082734768273477GA21GENIChomozygous45416641
2082734818273482CG24GENIChomozygous45416643
2082735138273514AC29GENIChomozygous45416645
2082736618273662AG20GENIChomozygous45416647
2082740178274018TTTC10GENICheterozygous45416649
2082753658275366CCTG8GENIChomozygous45841336
2082753978275398AG9GENIChomozygous45737353
2082754008275401CT9GENIChomozygous45737354
2082755048275505AACTTTTTTTTTTTGGTTCTTTTTTTTTTTTCGGAGCTGGGG4GENICheterozygous45841337
2082759888275992TAGT----15GENIChomozygous45416655
2082763358276336T-8GENICpossibly homozygous45416657
2082763608276361GT12GENIChomozygous45416659
2082764168276417AG18GENIChomozygous45416660
2082765258276526TTTG11GENICpossibly homozygous45416662
2082765868276587CT20GENIChomozygous45416664
2082767168276758TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC------------------------------------------7GENIChomozygous45841338
2082769828276983TC14GENIChomozygous45416666
2082778438277844GGGTGTGTGT5GENICheterozygous45841339
2082778438277844GGGTGTGTGTGT5GENICheterozygous45841340
2082780748278075CCGTGTGTGTGT9GENICheterozygous45416669
2082780748278075CCGTGTGTGTGTGT9GENICpossibly homozygous45841341
2082781008278110ACAGACAGAC----------10GENIChomozygous45416671
2082784098278410CT24GENIChomozygous45416675
2082788448278845TA21GENIChomozygous45416677
2082791898279190TTG6GENICheterozygous45841342
2082791998279200T-4GENICheterozygous45416682
2082793188279319AAGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAAGAAGCGCAAGGCCCTGG4GENIChomozygous45841343
2082795998279600GC13GENIChomozygous45416683
2082805248280525TC20GENIChomozygous45416685
2082809718280972CCTTTTTTT8GENIChomozygous45416688