chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135157095551570956GT20GENIChomozygous114948165
135157148451571485GT36GENIChomozygous114948167
135157164851571649GA30GENIChomozygous114948169
135157170051571701GA24GENIChomozygous114948171
135157180151571802AG22GENIChomozygous114948173
135157237851572379GA30GENICpossibly homozygous114948175
135157270451572705TC26GENIChomozygous114948177
135157279751572798CT22GENIChomozygous114948179
135157284051572841CT24GENIChomozygous114948181
135157296751572968CT27GENICpossibly homozygous114948183
135157324351573244AG38GENIChomozygous114948185
135157370451573705CT15GENIChomozygous114948187
135157641651576417TC22GENIChomozygous114343551
135157701051577011TC22GENIChomozygous114343553
135157739751577398CT19GENIChomozygous114948189
135157753751577538CT30GENIChomozygous114948191