chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110669704110669705TC43GENIChomozygous112003935
3110669764110669765AG46GENIChomozygous112003937
3110670472110670473CT47GENIChomozygous112139000
3110671832110671833GA47GENIChomozygous112003939
3110672581110672581A53GENIChomozygous130907827
3110672711110672712GC45GENIChomozygous112003943
3110673349110673350TA55GENIChomozygous111673167
3110674207110674208TC44GENICpossibly homozygous112139001
3110674208110674209GA45GENICpossibly homozygous112139002
3110674465110674466TC58GENIChomozygous111673170
3110674854110674855AG62GENIChomozygous111673172
3110676197110676198GT31GENIChomozygous111673173
3110676200110676201TA33GENIChomozygous111673175
3110676206110676207GT34GENIChomozygous111673177
3110679217110679218CT39GENIChomozygous111673183
3110684387110684388AC52GENIChomozygous111673190
3110684444110684445CT54GENIChomozygous112139003