chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84524174545241746AG8GENIChomozygous52615623
84524175345241754CCA10GENIChomozygous52615625
84524186645241867GA23GENIChomozygous52615627
84524202845242029AG23GENIChomozygous53317540
84524210445242105TTG16GENIChomozygous52615629
84524217845242179TC24GENIChomozygous52615631
84524262945242630GA22GENIChomozygous52615633
84524275745242758GA21GENIChomozygous52615635
84524284045242841GA27GENIChomozygous52615637
84524284845242849AC29GENIChomozygous52615639
84524294045242941CT25GENICpossibly homozygous52615641
84524297645242977GA22GENIChomozygous52615643
84524298545242986TC25GENIChomozygous52615645
84524313045243131AG22GENIChomozygous52615647
84524331145243312GA27GENIChomozygous52615649
84524357745243578AG16GENIChomozygous52615651
84524378345243784TTACACAC4GENIChomozygous53380093
84524416445244165A-13GENICpossibly homozygous52969496
84524453945244542GGG---8GENICheterozygous52969498
84524454045244542GG--8GENICpossibly homozygous52615657
84524468245244683CCCT6GENIChomozygous53317541
84524481645244817TC22GENIChomozygous52615663
84524488745244888CCTG13GENIChomozygous53317542
84524507045245071GA19GENIChomozygous53317543
84524541245245413CA20GENIChomozygous53317544
84524543645245437CT19GENIChomozygous53317545
84524543745245438AG18GENIChomozygous53317546
84524565445245655GA17GENIChomozygous53317547
84524565545245656CT17GENIChomozygous53317548
84524598145245982A-12GENIChomozygous53105817
84524624545246246AG18GENIChomozygous53105818
84524656445246565AG21GENIChomozygous52615667
84524672045246721CA21GENIChomozygous53317550
84524657045246571AG24GENIChomozygous53105819
84524661445246615CT25GENIChomozygous52615669
84524661845246619CT24GENIChomozygous53317549
84524698845246989G-19GENIChomozygous53317551
84524724845247249AG25GENIChomozygous52615671
84524725245247253AT27GENIChomozygous52615673
84524752445247525GA8GENIChomozygous53317552
84524753645247537AG10GENICpossibly homozygous53380097
84524774545247746TC17GENIChomozygous53317553