chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61575919015759191TC15GENIChomozygous115048169
61575941815759419AG19GENIChomozygous115048170
61576016615760167GA20GENIChomozygous115048171
61576135515761356TC8GENIChomozygous115048172
61576152715761528AT11GENIChomozygous115048173
61576191015761911AG19GENIChomozygous115048174
61576289715762898TA10GENIChomozygous115048175
61576331215763313GA15GENIChomozygous115048176
61576451715764518GC12GENIChomozygous115048177
61576570315765704AG29GENIChomozygous115048178
61576663615766637AC20GENIChomozygous115048179
61576949215769493AG13GENIChomozygous115048180
61577007215770073AG21GENIChomozygous115048181
61577097215770973GA11GENIChomozygous115048182
61577311715773118CA9GENIChomozygous115048183
61577311915773120AC12GENIChomozygous115048184
61577382715773828CT24GENIChomozygous115048185
61577637415776375GA25GENIChomozygous115048187
61577700415777005CA11GENIChomozygous115048188
61577737515777376CT26GENIChomozygous115048189
61577740515777406AG21GENIChomozygous115048190
61577774215777743AG18GENIChomozygous115048191
61577824715778248CT19GENIChomozygous115048192