chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85685850556858506GC11GENICheterozygous52980263
85685851256858513TC9GENICheterozygous52980264
85685881556858816TG6GENICheterozygous54409435
85685927356859274TC10GENICheterozygous52651612
85685929856859299AG13GENIChomozygous52651615
85685976256859763GA11GENIChomozygous52651618
85686020156860202TA9GENIChomozygous52651624
85686086356860864AG14GENIChomozygous52651627
85686154156861542TC18GENIChomozygous52651630
85686264056862641GGTGAATGAA12GENICheterozygous52980266
85686328656863287GA19GENICheterozygous52651633
85686361656863617G-15GENIChomozygous52651636
85686427056864271CT14GENICheterozygous52980268
85686474156864745TGAA----8GENIChomozygous52651651
85686507156865072T-14GENICheterozygous52980270
85686507356865074T-14GENICheterozygous52980271
85686717856867179AT20GENICheterozygous52980272
85686775756867758GT12GENICheterozygous52980273
85686778356867784TG14GENICheterozygous52980274
85686929456869295A-9GENICheterozygous54256001
85686944256869443CG13GENIChomozygous52651661
85686976256869763AG7GENIChomozygous52651667
85686979856869799CA9GENICheterozygous52980278
85687044456870445GA15GENICheterozygous52651669
85687045756870458GT13GENICheterozygous52651672
85687331756873318TC12GENICheterozygous52651678
85687374656873747CT16GENICheterozygous52980282
85687383056873831CG14GENICheterozygous52651692