chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171869549171869550TA11GENICheterozygous61961037
1171871053171871054AG19GENICpossibly homozygous60944010
1171873643171873644GA16GENICheterozygous61961038
1171873979171873980GA18GENICpossibly homozygous60944018
1171874164171874165CT29GENICpossibly homozygous61961039
1171875333171875334TC15GENIChomozygous60944021
1171875436171875437CT8GENIChomozygous60944022
1171875478171875479TC11GENICpossibly homozygous60944023
1171875760171875761AC10GENIChomozygous60944024
1171876014171876015GGT16GENIChomozygous61961040
1171877208171877209TC14GENIChomozygous60944026
1171877735171877736AG4GENIChomozygous60944027
1171879092171879093AC13GENIChomozygous61556163
1171879418171879419CT9GENIChomozygous61961041
1171879430171879431TC12GENICpossibly homozygous61556164
1171879710171879711CT22GENIChomozygous61556165
1171880218171880219AG8GENICpossibly homozygous61556166
1171880550171880551CT9GENIChomozygous61556167
1171880832171880833GA9GENIChomozygous61556168
1171880856171880857GA13GENIChomozygous61556169
1171881567171881568AG11GENIChomozygous60944035
1171882823171882824GGA2GENIChomozygous60944037
1171883105171883106G-16GENIChomozygous61556171
1171884278171884279AG10GENIChomozygous60944041