chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99391541193915412AT24INTERGENIChomozygous69041398
99391555693915557AG29INTERGENIChomozygous69041402
99391583793915838GA31INTERGENIChomozygous69041408
99391591793915918GA27INTERGENIChomozygous69041412
99391612993916130GA32INTERGENIChomozygous69041415
99391630893916309GC28INTERGENIChomozygous69218940
99391645393916454GA23INTERGENIChomozygous69921793
99391616993916170CA25INTERGENIChomozygous69921781
99391645293916453TC23INTERGENIChomozygous69921790
99391646593916466AG21INTERGENIChomozygous68201923
99391660293916603TC10INTERGENIChomozygous68201931
99391665593916656GT17INTERGENIChomozygous69041424
99391673093916731GA12INTERGENIChomozygous69218942
99391673493916735CT9INTERGENIChomozygous69218943
99391675693916757TC14INTERGENIChomozygous68201934
99391682793916828GA26INTERGENIChomozygous69041428
99391700193917002AG17INTERGENICpossibly homozygous69218944
99391710393917104GA22INTERGENIChomozygous70007551
99391710793917108GT20INTERGENIChomozygous69218945
99391724693917247AG30INTERGENIChomozygous69218946
99391725893917259TC35INTERGENIChomozygous69041433
99391734393917344AG32INTERGENIChomozygous69041436
99391739893917399AG35INTERGENIChomozygous69218947
99391747693917477TA34INTERGENIChomozygous69041440
99391747893917479TC35INTERGENIChomozygous69218948
99391750793917508CG41INTERGENIChomozygous69041444
99391758893917589GA34INTERGENIChomozygous69041448
99391763193917632CT30INTERGENIChomozygous69041452
99391765193917652TC35INTERGENIChomozygous69041457
99391776693917767TG34INTERGENIChomozygous69921805
99391776993917770AT33INTERGENIChomozygous69041461
99391777293917773CT29INTERGENIChomozygous69041465
99391779793917798AG20INTERGENIChomozygous69218949
99391782393917824TC31INTERGENIChomozygous68201936
99391790493917905GA26INTERGENIChomozygous69041469
99391791193917912TC23INTERGENIChomozygous69041473
99391796093917961GA42INTERGENIChomozygous69041477
99391800193918002GA39INTERGENIChomozygous69041481
99391707493917075GA17INTERGENIChomozygous82538627