chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178138830178138831AAT2GENIChomozygous62178790
1178139420178139421AAGTGAAAGTGATTGTTGGGGG2GENIChomozygous61312694
1178140114178140115T-27GENIChomozygous60971165
1178140178178140179TC26GENIChomozygous61562492
1178141737178141738AC7GENIChomozygous61562494
1178141937178141938TC14GENIChomozygous60971173
1178141978178141979AG13GENIChomozygous60971175
1178141990178141991AG15GENIChomozygous61562495
1178142460178142461GC15GENIChomozygous61562496
1178142618178142619AAT20GENIChomozygous61562497
1178142940178142941GT22GENIChomozygous60971181
1178142953178142954TA21GENIChomozygous60971183
1178142986178142987TTACACACAC6GENIChomozygous61562498
1178143212178143213GA29GENIChomozygous60971187
1178144831178144832GT19INTERGENIChomozygous61562499
1178145206178145207CT21INTERGENIChomozygous61562500
1178145483178145484AAT27INTERGENIChomozygous61562501
1178145719178145725AAAAAA------23INTERGENICpossibly homozygous61562503
1178179910178179911GT8INTERGENIChomozygous61562504
1178179994178179995A-10INTERGENICpossibly homozygous62178792
1178186866178186867AC26INTERGENIChomozygous61562505
1178190806178190807T-19INTERGENIChomozygous62091923
1178191271178191272AAAT19INTERGENIChomozygous60971222