chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125048666125048667TC27GENIChomozygous54095975
7125048786125048787GA37GENIChomozygous54751193
7125048936125048937GT42GENIChomozygous54095976
7125049753125049759CAAAAA------13GENICpossibly homozygous54751195
7125050478125050479GT25GENIChomozygous54095985
7125052214125052215TTGGAG7GENIChomozygous54095989
7125052304125052305CT8GENIChomozygous54751197
7125054097125054098GC25GENIChomozygous54751201
7125055836125055837GC20GENIChomozygous54751203
7125055845125055846AG23GENIChomozygous54095994
7125055846125055847TTG23GENIChomozygous54751205
7125055851125055852AG22GENIChomozygous54095995
7125057462125057463AG21GENIChomozygous54095997
7125057782125057783CT27GENIChomozygous54751207
7125058073125058097TGGGGCAGGCTGTGGGGCAGGCTG------------------------12GENIChomozygous55004882
7125058254125058255CT19GENIChomozygous54751209
7125058519125058520TC23GENIChomozygous54095998
7125059731125059732GGC25GENIChomozygous54096000
7125062164125062165GA16GENIChomozygous54751211
7125063395125063396GA15GENIChomozygous54751213
7125063609125063610GA20GENIChomozygous54751215
7125065231125065232TC22GENIChomozygous54096018
7125066925125066926GC15GENIChomozygous54096020
7125066951125066952TA17GENIChomozygous54751217
7125068721125068722TC18GENIChomozygous54096027
7125070527125070528TG14GENIChomozygous54096029
7125063192125063200TGTGTGTG--------5GENIChomozygous55097703