chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97960234879602349CT20GENIChomozygous117578568
97960476779604768AG5GENIChomozygous117380740
97960563479605635GT30GENIChomozygous117578580
97961835779618358GC6GENIChomozygous117578608
97961979979619800TG19GENIChomozygous117729484
97961090479610905AG11GENIChomozygous117729478
97961832679618327GT13GENIChomozygous117729480
97961963879619639AG27GENIChomozygous117729482
97962053979620540AG18GENIChomozygous117729486
97962065279620653AG14GENIChomozygous117729488
97962091479620915CT15GENIChomozygous117729490
97962110179621102AG18GENIChomozygous117578612
97962240179622402CT23GENIChomozygous117729492
97962243579622436GA24GENIChomozygous117729494
97962255979622560TC19GENIChomozygous117578616
97962283679622837GA20GENIChomozygous117729496
97962552379625524TC12GENIChomozygous117729498
97962595079625951TC9GENIChomozygous117794123
97962606679626067CT13GENIChomozygous117729500
97962675879626759CA14GENIChomozygous117578634
97962731079627311CG19GENIChomozygous117578636
97962734179627342GT22GENIChomozygous117578638
97962766679627667CG10GENIChomozygous117578642
97962805179628052AT6GENIChomozygous117578644
97962850479628505TC17GENIChomozygous117578646
97962856579628566AC17GENIChomozygous117578648
97962877579628776CA22GENIChomozygous117578650
97962883279628833CT23GENIChomozygous117578652
97962909079629091CT18GENIChomozygous117578654
97962926279629263CT22GENIChomozygous117578656
97962968079629681AT13GENIChomozygous117578660
97962969279629693CT12GENIChomozygous117578662