chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142307157142307158CT19GENIChomozygous116097718
7142308425142308426CT16GENIChomozygous115941717
7142308713142308714GA22GENIChomozygous115941718
7142310471142310472TG10GENIChomozygous116097720
7142310688142310689TC6GENIChomozygous115941719
7142310811142310812AC15GENIChomozygous115941720
7142310892142310893GA16GENIChomozygous115941721
7142308119142308120TA19GENIChomozygous118261073
7142310919142310919T20GENIChomozygous131025790
7142310928142310928T24GENIChomozygous131025791
7142311316142311317AG17GENIChomozygous116097722
7142311727142311728CT19GENIChomozygous116097724
7142312201142312201G9GENIChomozygous130347259
7142312252142312252GAC3GENIChomozygous128530452
7142312176142312177C10GENIChomozygous128530450
7142312191142312191C9GENIChomozygous128530451
7142312258142312258T3GENIChomozygous128530453
7142312263142312263C3GENIChomozygous128530454
7142312275142312278AGA2GENIChomozygous128530455
7142312281142312281GGT2GENIChomozygous128530456
7142312288142312289T1GENIChomozygous128530457
7142313489142313490CG14GENIChomozygous115941729
7142313528142313529TC12GENIChomozygous115941730
7142313902142313903AT16GENIChomozygous116097726
7142315146142315147TA16GENIChomozygous116097728
7142315308142315309AG20GENIChomozygous116097730
7142315783142315784CT24GENIChomozygous116097732
7142316042142316043CT12GENIChomozygous115941738
7142316090142316090C13GENIChomozygous128530467
7142312286142312287CT1GENIChomozygous118434121
7142318518142318519TC25GENIChomozygous115941747
7142318531142318532TC20GENIChomozygous115941748