chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104795209847952099AG15GENIChomozygous116588161
104795221747952218GA15GENIChomozygous116588165
104795256247952563CT14GENIChomozygous116878983
104795282047952820AAGGGCTGAGT15GENIChomozygous131092761
104795365547953656GA18GENIChomozygous116878985
104795617847956179GA11GENIChomozygous116878987
104795950347959504TA18GENIChomozygous116588169
104796009147960094AGG20GENIChomozygous131092762
104796197447961975CG11GENIChomozygous116588171
104796332947963330TC21GENIChomozygous116588177
104796458147964582AG16GENIChomozygous116588179
104796607647966077AG14GENIChomozygous116878989
104796664247966643GA7GENIChomozygous117129099
104796847347968474TG16GENIChomozygous116588183
104796921247969212TTG9GENIChomozygous131092763
104797092347970924TC19GENIChomozygous116878991
104797141247971413GA12GENIChomozygous116878993
104797547547975476AG18GENIChomozygous116588187
104797711247977113TC29GENIChomozygous116588189
104797970947979710GC14GENIChomozygous116878995
104798596747985968TC16GENIChomozygous116588191
104798641847986419AG12GENIChomozygous116878997
104798685747986858TC23GENIChomozygous116878999
104798725647987257AG16GENIChomozygous116588193
104798730047987301CT17GENIChomozygous116588195
104798853247988533CT12GENIChomozygous117059163
104799040947990410CT9GENIChomozygous116879001
104799199447991995GA18GENIChomozygous116879003
104799420647994207GA14GENIChomozygous116879005
104795793547957940ACTTA16GENIChomozygous128814996
104795794247957942GTC16GENIChomozygous128814997
104797536247975362C18GENIChomozygous128814999
104799438947994389C3GENIChomozygous128815002
104799438947994390GT3GENIChomozygous116774451