chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171869549171869550TA14GENICpossibly homozygous61961037
1171871053171871054AG25GENIChomozygous60944010
1171873643171873644GA20GENICpossibly homozygous61961038
1171873979171873980GA21GENIChomozygous60944018
1171874164171874165CT27GENIChomozygous61961039
1171875333171875334TC8GENIChomozygous60944021
1171875436171875437CT8GENIChomozygous60944022
1171875478171875479TC13GENIChomozygous60944023
1171875760171875761AC15GENIChomozygous60944024
1171876014171876015GGT12GENICheterozygous61961040
1171877208171877209TC16GENIChomozygous60944026
1171877735171877736AG14GENIChomozygous60944027
1171878553171878555AA--2GENIChomozygous61556162
1171879092171879093AC11GENICheterozygous61556163
1171879418171879419CT21GENICpossibly homozygous61961041
1171879430171879431TC16GENIChomozygous61556164
1171879710171879711CT20GENIChomozygous61556165
1171880218171880219AG23GENICpossibly homozygous61556166
1171880550171880551CT14GENICpossibly homozygous61556167
1171880832171880833GA22GENICpossibly homozygous61556168
1171880856171880857GA11GENIChomozygous61556169
1171881567171881568AG20GENICpossibly homozygous60944035
1171883105171883106G-19GENIChomozygous61556171
1171884278171884279AG18GENICpossibly homozygous60944041