chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
82298747022987471AACT19GENIChomozygous52537165
82298771922987720GGT18GENICheterozygous53096618
82298772022987721T-18GENICheterozygous53615573
82298794622987947CT15GENIChomozygous52537167
82298798522987986TTC10GENIChomozygous52537169
82298809022988091GGT13GENICpossibly homozygous52537171
82298953222989533CT32GENIChomozygous52537173
82299013722990138GGA21GENIChomozygous52537175
82299037822990379TC17GENIChomozygous52537177
82298821722988218CCGT2GENIChomozygous53602073
82299014322990144GA23GENIChomozygous53535356
82299101422991015AATATGTATG3GENIChomozygous53602075
82299116522991166CT13GENIChomozygous52537181
82299149522991496TC22GENIChomozygous52537183
82299246122992462C-23GENIChomozygous52537185
82299246222992463CT21GENIChomozygous53535357