chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142307157142307158CT56GENIChomozygous116097718
7142308425142308426CT52GENIChomozygous115941717
7142308713142308714GA47GENIChomozygous115941718
7142310471142310472TG53GENIChomozygous116097720
7142310671142310672GT16GENICheterozygous122877797
7142310688142310689TC15GENIChomozygous115941719
7142310811142310812AC38GENIChomozygous115941720
7142310892142310893GA38GENIChomozygous115941721
7142311316142311317AG43GENIChomozygous116097722
7142311727142311728CT46GENIChomozygous116097724
7142312275142312278AGA7GENIChomozygous128530455
7142308119142308120TA43GENIChomozygous118261073
7142310919142310919T37GENIChomozygous131025790
7142310928142310928T42GENIChomozygous131025791
7142312176142312177C21GENIChomozygous128530450
7142312191142312191C18GENIChomozygous128530451
7142312252142312252GAC10GENIChomozygous128530452
7142312258142312258T9GENIChomozygous128530453
7142312263142312263C8GENIChomozygous128530454
7142312201142312201G18GENIChomozygous130347259
7142312281142312281GGT6GENIChomozygous128530456
7142312288142312289T5GENIChomozygous128530457
7142312302142312302T3GENIChomozygous128530458
7142312306142312307C2GENIChomozygous128530459
7142313489142313490CG61GENIChomozygous115941729
7142313528142313529TC57GENIChomozygous115941730
7142313902142313903AT50GENIChomozygous116097726
7142315146142315147TA44GENIChomozygous116097728
7142315308142315309AG53GENIChomozygous116097730
7142315783142315784CT61GENIChomozygous116097732
7142316042142316043CT33GENIChomozygous115941738
7142316090142316090C26GENIChomozygous128530467
7142312286142312287CT5GENIChomozygous118434121
7142318518142318519TC42GENIChomozygous115941747
7142318531142318532TC40GENIChomozygous115941748