chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61575919015759191TC22GENIChomozygous115048169
61575941815759419AG25GENIChomozygous115048170
61576016615760167GA29GENIChomozygous115048171
61576135515761356TC3GENIChomozygous115048172
61576152715761528AT7GENIChomozygous115048173
61576191015761911AG16GENIChomozygous115048174
61576289715762898TA22GENIChomozygous115048175
61576331215763313GA37GENIChomozygous115048176
61576451715764518GC22GENIChomozygous115048177
61576570315765704AG27GENIChomozygous115048178
61576663615766637AC37GENIChomozygous115048179
61576949215769493AG24GENIChomozygous115048180
61577007215770073AG12GENIChomozygous115048181
61577097215770973GA9GENIChomozygous115048182
61577382715773828CT16GENIChomozygous115048185
61577637415776375GA17GENIChomozygous115048187
61577700415777005CA23GENIChomozygous115048188
61577737515777376CT16GENIChomozygous115048189
61577740515777406AG20GENIChomozygous115048190
61577774215777743AG26GENIChomozygous115048191
61577824715778248CT14GENIChomozygous115048192