chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71244092912440930AG17GENIChomozygous54630355
71244107012441071TC13GENIChomozygous53790948
71244240812442409T-10GENIChomozygous53790951
71244280812442809AAC20GENIChomozygous53790952
71244289712442905TCTGAGTT--------11GENIChomozygous53790953
71244302412443025TC17GENIChomozygous53790954
71244315612443159TTT---10GENIChomozygous53790955
71244316012443161TG10GENIChomozygous54884988
71244334412443345T-11GENIChomozygous53790956
71244434612444347TG9GENIChomozygous53790960
71244466712444668AG7GENIChomozygous53790961
71244514512445146CT13GENIChomozygous53790962
71244522712445228TC11GENIChomozygous53790963
71244549212445493TC14GENIChomozygous53790965
71244549512445496TG14GENIChomozygous53790966
71244550512445506CG15GENIChomozygous53790967
71244840012448401CT7GENIChomozygous53790978
71244857512448576TC8GENIChomozygous53790979
71244904712449048AG13GENIChomozygous53790981
71245007112450072CT8GENIChomozygous53790983
71245049912450500AG11INTERGENIChomozygous53790984
71245064312450644AAATAC11INTERGENIChomozygous53790985
71245080512450806CT11INTERGENIChomozygous53790986
71245097312450974AG13INTERGENIChomozygous54630359
71245139512451396A-10INTERGENIChomozygous53790987
71245157312451574CT18INTERGENIChomozygous54630361
71245173112451732GC12INTERGENIChomozygous54630363
71245213312452134GT12GENIChomozygous54630365
71245241912452420GC10GENIChomozygous54630367