chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118216161982161620GA21GENIChomozygous139030151
118216212082162121CT18GENIChomozygous139030152
118216343282163433AG28GENIChomozygous139030153
118216376682163767GA27GENIChomozygous139030154
118216414282164143TC18GENIChomozygous139030155
118216624582166246TC28GENIChomozygous139030156
118216711382167114GA28GENIChomozygous139030157
118216740882167409CT25GENICpossibly homozygous139030158
118216858482168585TC12GENIChomozygous139030159
118217067982170680CT20GENIChomozygous139030160
118217128882171289TC12GENIChomozygous139030161
118217183282171833CT16GENIChomozygous139030162
118217241882172419CG29GENIChomozygous139030163
118217296882172969AT21GENICpossibly homozygous139030164
118217297382172974CA23GENICpossibly homozygous139030165
118217300182173002CT23GENICpossibly homozygous139030166
118217195882171958A22GENIChomozygous138897648
118217509982175101CA27GENICpossibly homozygous138897649
118217605182176052CA18GENIChomozygous139030171
118217665082176651CA16GENIChomozygous139030172
118217750782177508TC14GENIChomozygous139030173
118217795682177957CT21GENIChomozygous139030174
118217811582178116GC15GENIChomozygous139030175
118217857082178571CT18GENIChomozygous139030176
118217867982178680CT24GENIChomozygous139030177
118217919582179196AG30GENIChomozygous139030178
118218030382180304GA17GENIChomozygous139030179
118218167582181676AG19GENIChomozygous139030180
118218292082182921CG21GENIChomozygous139030181
118218499682184997AG23GENIChomozygous139030182
118217480582174806GA2GENIChomozygous140907341