chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763972417639725TC20GENIChomozygous973722100
141764052517640526TC24GENIChomozygous973722101
141764261817642619CT29GENIChomozygous973722102
141764265617642657CA29GENIChomozygous973722103
141764342217643423GC18GENIChomozygous973722104
141764352417643525CT27GENIChomozygous973722105
141764359417643595CA12GENIChomozygous973722106
141764416617644167GT21GENIChomozygous973722107
141764622417646225CT29GENIChomozygous973722108
141764987017649871CA22GENIChomozygous973722109
141765004317650044CT21GENIChomozygous973722110
141765048617650487CT11GENIChomozygous973722111
141765054617650547TC23GENIChomozygous973722112
141765054917650550CT24GENIChomozygous973722113
141765055317650554GA24GENIChomozygous973722114
141765061417650615CT23GENIChomozygous973722115
141765064217650643AT23GENIChomozygous973722116
141765064417650645AT21GENIChomozygous973722117
141765067217650673TG26GENIChomozygous973722118
141765072117650722AG28GENIChomozygous973722119
141765073017650731CT29GENIChomozygous973722120
141765112317651124TA13GENIChomozygous973722121
141765115717651158AT21GENIChomozygous973722122
141765116317651164GA21GENIChomozygous973722123
141765141217651413AT12GENIChomozygous973722124
141765144717651448TG13GENIChomozygous973722125
141765161617651617AG16GENIChomozygous973722126
141765171117651712GC13GENIChomozygous973722127
141765171817651719GA16GENIChomozygous973722128
141765172617651727GT17GENIChomozygous973722129
141765179617651797GA10GENIChomozygous973722130
141765438217654383CA17GENIChomozygous973722131
141765581617655817TC23GENIChomozygous973722132
141765645617656457TC24GENIChomozygous973722133
141765649817656499CT22GENIChomozygous973722134
141765685017656851AG16GENICpossibly homozygous973722135