chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185634369656343696A12GENICheterozygous131206355
185635302056353020TCCAAAGAAGACTGCAAGC4GENIChomozygous129540801
185635320556353205G9GENIChomozygous129540802
185635324156353242G8GENIChomozygous129540803
185635324856353248G8GENIChomozygous129540804
185635347656353476T3GENIChomozygous129540806
185635523256355233TG11GENIChomozygous110361500
185635534256355343CG9GENIChomozygous110631238
185635527356355274TC8GENIChomozygous110361502
185635527756355278TG8GENIChomozygous110361504
185635531556355316TA11GENIChomozygous110361506
185635534456355345TG8GENIChomozygous110631240
185635534656355347T8GENIChomozygous129540809
185635534856355349TG7GENIChomozygous110631242
185635535056355355TGTTT7GENIChomozygous129540810
185635535556355356TC7GENIChomozygous110631244
185635535956355360TG7GENIChomozygous110631246
185635536256355362CCC7GENIChomozygous129540811
185635536556355373TGTGTGTT7GENIChomozygous129540812
185635537856355385TTTTTTT6GENIChomozygous129540813
185635538656355391TTTTT6GENIChomozygous129540814
185635539956355401TT6GENIChomozygous129540815
185635540256355403G6GENIChomozygous129540816
185635541056355411TA8GENIChomozygous124478323
185635541256355414TT8GENIChomozygous129540817
185635542056355422GA10GENIChomozygous129540818
185635542956355436TTTTTTT10GENIChomozygous129540819
185635543756355437CC9GENIChomozygous129540820
185635544856355448G10GENIChomozygous129540821