chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
499370719937072AG22GENIChomozygous954698137
499370759937076TC21GENIChomozygous954698138
499372749937275GA31GENIChomozygous954698139
499372869937287CT33GENIChomozygous954698140
499372989937299GA33GENIChomozygous954698141
499373219937322GA38GENIChomozygous954698142
499373999937400GA31GENIChomozygous954698143
499374609937461CA34GENIChomozygous954698144
499375489937549CT24GENIChomozygous954698145
499376549937655TG20GENIChomozygous954698146
499377019937702GA16GENIChomozygous954698147
499377219937722GA17GENIChomozygous954698148
499377349937735AC17GENIChomozygous954698149
499377469937747AG15GENIChomozygous954698150
499379589937959GT29GENIChomozygous954698151
499380479938048CG33GENIChomozygous954698152
499381759938176AG32GENIChomozygous954698153
499382179938218TA24GENIChomozygous954698154
499382519938252TA25GENIChomozygous954698155
499384169938417CG21GENIChomozygous954698156
499384349938435GT20GENIChomozygous954698157
499384509938451TC19GENIChomozygous954698158
499384829938483GT19GENIChomozygous954698159
499388009938801GT21GENIChomozygous954698160
499388499938850CT31GENIChomozygous954698161
499388799938880AG34GENIChomozygous954698162
499388879938888GC38GENIChomozygous954698163