chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139242773139242774AC5GENIChomozygous55749067
5139242777139242779AT--6GENIChomozygous55749068
5139244152139244153TA2GENIChomozygous55749070
5139245509139245510TC20GENIChomozygous55749071
5139245828139245829GGTC18GENICpossibly homozygous55749072
5139246651139246652CT2GENIChomozygous55749073
5139247962139247963AG1GENIChomozygous55749074
5139249651139249652AT6GENICheterozygous55749078
5139250149139250150AG20GENIChomozygous55749080
5139251457139251458CT9GENICpossibly homozygous55749081
5139253038139253039CA7GENIChomozygous55749083
5139253793139253795AA--11GENIChomozygous55749086
5139255721139255722T-1GENIChomozygous55749087
5139257031139257032CT15GENIChomozygous55749091
5139257553139257554TG15GENIChomozygous55749093
5139257697139257698A-3GENIChomozygous55749094
5139258123139258124AAT2GENIChomozygous55749095
5139258128139258129AAAATAAAAAAAT3GENIChomozygous55749096
5139260072139260073GA9GENIChomozygous55749100
5139260216139260217GA14GENIChomozygous55749101
5139260735139260736AG15GENICpossibly homozygous55749102
5139260910139260911A-3GENIChomozygous55749103
5139263436139263437TC14GENIChomozygous55749107
5139264975139264976TG21GENIChomozygous55749109
5139265823139265824A-3GENICheterozygous56354980
5139265976139265977AG18GENICpossibly homozygous55749113
5139266379139266380GA4GENIChomozygous55749116
5139267618139267619AG11GENICpossibly homozygous55749117
5139267995139267996AG4GENICheterozygous55749118