chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101526566615265667T-31GENIChomozygous51624349
101526631415266315GA48GENICheterozygous51624350
101526677915266780GGAGAGAGAA35GENICheterozygous51624351
101526718815267189GA32GENICheterozygous51624352
101526721115267228CCAAGGACATGGGGACC-----------------11GENICpossibly homozygous51624353
101526741315267414CT43GENIChomozygous51624354
101526763015267631AG66GENIChomozygous51624355
101526769615267697T-41GENIChomozygous51624356
101526851515268516AG40GENIChomozygous51624357
101526879915268800CCA27GENICpossibly homozygous51624358
101526934215269343CT53GENICpossibly homozygous51624359
101526946215269463GT53GENICpossibly homozygous51624360
101527234615272347CT30GENICpossibly homozygous51624361
101526677515266776AAAG7GENIChomozygous51331012
101527285915272860CCGATA26GENIChomozygous51331013
101527290015272901GGATAA51GENICheterozygous51331014