chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84524174545241746AG17GENICpossibly homozygous52615623
84524175345241754CCA17GENIChomozygous52615625
84524186645241867GA21GENIChomozygous52615627
84524210445242105TTG32GENIChomozygous52615629
84524217845242179TC23GENIChomozygous52615631
84524262945242630GA23GENIChomozygous52615633
84524275745242758GA36GENIChomozygous52615635
84524284045242841GA29GENIChomozygous52615637
84524284845242849AC30GENIChomozygous52615639
84524294045242941CT25GENIChomozygous52615641
84524297645242977GA27GENIChomozygous52615643
84524298545242986TC29GENIChomozygous52615645
84524313045243131AG24GENIChomozygous52615647
84524331145243312GA33GENIChomozygous52615649
84524357745243578AG31GENIChomozygous52615651
84524378345243784TTACAC8GENICheterozygous52615653
84524378345243784TTACACAC8GENICheterozygous53380093
84524378345243784TTACACACACAC8GENICheterozygous53380095
84524454045244542GG--26GENIChomozygous52615657
84524467445244675AAC11GENICpossibly homozygous52615659
84524472045244721TC25GENIChomozygous52615661
84524481645244817TC16GENIChomozygous52615663
84524598045245981TTA20GENIChomozygous52615665
84524656445246565AG28GENIChomozygous52615667
84524661445246615CT21GENIChomozygous52615669
84524724845247249AG22GENIChomozygous52615671
84524725245247253AT24GENIChomozygous52615673
84524753645247537AG1GENIChomozygous53380097