chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125048666125048667TC20GENIChomozygous54095975
7125048786125048787GA32GENICpossibly homozygous54751193
7125048936125048937GT24GENIChomozygous54095976
7125049753125049757CAAA----19GENICheterozygous54095981
7125049753125049759CAAAAA------19GENICheterozygous54751195
7125050478125050479GT51GENIChomozygous54095985
7125052214125052215TTGGAG8GENIChomozygous54095989
7125052304125052305CT18GENIChomozygous54751197
7125054097125054098GC40GENIChomozygous54751201
7125055836125055837GC30GENICpossibly homozygous54751203
7125055845125055846AG35GENIChomozygous54095994
7125055846125055847TTG35GENICpossibly homozygous54751205
7125055851125055852AG36GENIChomozygous54095995
7125057462125057463AG28GENIChomozygous54095997
7125057782125057783CT17GENIChomozygous54751207
7125058073125058097TGGGGCAGGCTGTGGGGCAGGCTG------------------------7GENIChomozygous55004882
7125058254125058255CT21GENIChomozygous54751209
7125058519125058520TC40GENIChomozygous54095998
7125059731125059732GGC20GENIChomozygous54096000
7125062164125062165GA21GENIChomozygous54751211
7125063395125063396GA19GENICpossibly homozygous54751213
7125063555125063556T-14GENICheterozygous54096015
7125063609125063610GA18GENICpossibly homozygous54751215
7125065231125065232TC19GENIChomozygous54096018
7125066925125066926GC26GENICpossibly homozygous54096020
7125066951125066952TA31GENICpossibly homozygous54751217
7125068721125068722TC30GENIChomozygous54096027
7125070527125070528TG20GENIChomozygous54096029
7125052362125052367AAGAT-----2GENIChomozygous55097701
7125063192125063200TGTGTGTG--------5GENIChomozygous55097703