chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142307157142307158CT50GENIChomozygous116097718
7142308425142308426CT53GENIChomozygous115941717
7142308713142308714GA31GENIChomozygous115941718
7142310471142310472TG49GENICpossibly homozygous116097720
7142310688142310689TC19GENIChomozygous115941719
7142310811142310812AC55GENIChomozygous115941720
7142310892142310893GA55GENIChomozygous115941721
7142308119142308120TA41GENIChomozygous118261073
7142310919142310919T53GENIChomozygous131025790
7142311316142311317AG51GENIChomozygous116097722
7142311727142311728CT58GENIChomozygous116097724
7142312258142312258T10GENIChomozygous128530453
7142310928142310928T50GENIChomozygous131025791
7142312191142312191C28GENIChomozygous128530451
7142312176142312177C29GENIChomozygous128530450
7142312252142312252GAC11GENIChomozygous128530452
7142312201142312201G25GENIChomozygous130347259
7142312263142312263C9GENIChomozygous128530454
7142312275142312278AGA8GENIChomozygous128530455
7142312281142312281GGT7GENIChomozygous128530456
7142312288142312289T5GENIChomozygous128530457
7142312302142312302T1GENIChomozygous128530458
7142312306142312307C1GENIChomozygous128530459
7142313489142313490CG69GENIChomozygous115941729
7142313528142313529TC63GENIChomozygous115941730
7142313902142313903AT59GENIChomozygous116097726
7142312286142312287CT5GENIChomozygous118434121
7142315146142315147TA56GENIChomozygous116097728
7142315308142315309AG67GENIChomozygous116097730
7142315783142315784CT44GENIChomozygous116097732
7142316042142316043CT34GENIChomozygous115941738
7142316090142316090C22GENIChomozygous128530467
7142318518142318519TC61GENIChomozygous115941747
7142318531142318532TC60GENIChomozygous115941748