chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212655812212655813GA18GENIChomozygous625978790
1212658705212658706GA16GENIChomozygous625978791
1212659762212659763TG11GENIChomozygous625978792
1212659968212659969AAT20GENIChomozygous742968977
1212661571212661572GT36GENIChomozygous625978793
1212662522212662523AAT15GENICheterozygous742968978
1212662522212662523AATT15GENICheterozygous742968979
1212662934212662935T-14GENIChomozygous742968980
1212663465212663466CT36GENIChomozygous625978794
1212664831212664832CT29GENIChomozygous625978795
1212666283212666284AG27GENIChomozygous625978796
1212666736212666737CCAG25GENICpossibly homozygous742968981
1212669279212669280TC23GENIChomozygous625978797
1212669743212669744AG18GENIChomozygous625978798
1212670030212670031AG34GENIChomozygous625978799
1212670346212670347CG44GENIChomozygous625978800
1212671116212671117CT23GENIChomozygous625978801
1212671289212671290CCTT6GENICheterozygous742968982
1212671289212671290CCTTTT6GENICheterozygous742968983
1212674420212674421GA16GENIChomozygous625978802
1212674751212674752T-22GENIChomozygous742968984
1212676526212676527GA19GENIChomozygous625978803
1212676698212676699GGTTGT25GENICpossibly homozygous742968985
1212678348212678351AGG---9GENICheterozygous742968987
1212680462212680463CT31GENIChomozygous625978804
1212681105212681229AAAAACACGTGAGTCCGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA----------------------------------------------------------------------------------------------------------------------------17GENIChomozygous742968988
1212685080212685081GA31GENIChomozygous625978805
1212688791212688792TC33GENIChomozygous625978806