chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125048666125048667TC8GENIChomozygous54095975
7125048786125048787GA10GENIChomozygous54751193
7125048936125048937GT13GENIChomozygous54095976
7125049753125049759CAAAAA------6GENICheterozygous54751195
7125050478125050479GT9GENIChomozygous54095985
7125052214125052215TTGGAG3GENIChomozygous54095989
7125052304125052305CT9GENIChomozygous54751197
7125054097125054098GC7GENIChomozygous54751201
7125055836125055837GC13GENIChomozygous54751203
7125055845125055846AG9GENIChomozygous54095994
7125055846125055847TTG10GENIChomozygous54751205
7125055851125055852AG10GENIChomozygous54095995
7125057462125057463AG8GENIChomozygous54095997
7125057782125057783CT12GENIChomozygous54751207
7125058073125058097TGGGGCAGGCTGTGGGGCAGGCTG------------------------4GENIChomozygous55004882
7125058254125058255CT8GENIChomozygous54751209
7125058519125058520TC3GENIChomozygous54095998
7125059731125059732GGC7GENIChomozygous54096000
7125062164125062165GA5GENIChomozygous54751211
7125063395125063396GA8GENIChomozygous54751213
7125063609125063610GA10GENIChomozygous54751215
7125065231125065232TC6GENIChomozygous54096018
7125066925125066926GC6GENIChomozygous54096020
7125066951125066952TA6GENIChomozygous54751217
7125068721125068722TC5GENIChomozygous54096027
7125070527125070528TG5GENIChomozygous54096029
7125052362125052367AAGAT-----3GENICheterozygous55097701
7125063192125063200TGTGTGTG--------3GENIChomozygous55097703