chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
61575919015759191TC18GENIChomozygous115048169
61575941815759419AG25GENIChomozygous115048170
61576016615760167GA24GENIChomozygous115048171
61576135515761356TC4GENICheterozygous115048172
61576152715761528AT11GENIChomozygous115048173
61576191015761911AG17GENIChomozygous115048174
61576289715762898TA28GENIChomozygous115048175
61576331215763313GA25GENIChomozygous115048176
61576451715764518GC29GENIChomozygous115048177
61576570315765704AG17GENIChomozygous115048178
61576663615766637AC26GENIChomozygous115048179
61576949215769493AG15GENIChomozygous115048180
61577007215770073AG8GENIChomozygous115048181
61577062115770622AT6GENICheterozygous118626735
61577062215770623GC6GENICheterozygous118626736
61577097215770973GA19GENIChomozygous115048182
61577382715773828CT12GENIChomozygous115048185
61577637415776375GA13GENIChomozygous115048187
61577700415777005CA11GENIChomozygous115048188
61577737515777376CT13GENIChomozygous115048189
61577740515777406AG13GENIChomozygous115048190
61577774215777743AG13GENIChomozygous115048191
61577824715778248CT18GENIChomozygous115048192