chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3146486525146486526GA56GENIChomozygous112185135
3146486589146486590TC49GENIChomozygous112185136
3146491445146491446TA45GENIChomozygous112185137
3146491598146491599GT69GENIChomozygous112185138
3146491921146491922TC53GENIChomozygous112185139
3146491930146491931TC58GENIChomozygous112185140
3146492173146492174GA51GENIChomozygous112185141
3146492229146492230CT52GENIChomozygous112185142
3146492452146492453GA61GENIChomozygous112185143
3146492483146492484GA65GENIChomozygous112185144
3146492886146492887AG57GENIChomozygous112185145
3146492967146492968AG52GENIChomozygous112185146
3146493201146493202AG51GENIChomozygous112185147
3146493298146493299AC51GENIChomozygous112185148
3146493984146493985AG42GENIChomozygous112185149
3146494103146494104CT34GENIChomozygous112185150
3146494182146494182A15GENIChomozygous127939733
3146494185146494186GT15GENIChomozygous111767720
3146494314146494315TC35GENICpossibly homozygous112185151
3146494510146494511GA45GENIChomozygous112185152
3146494194146494204CCACCCACAG15GENIChomozygous130913751