chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142225155142225156TA34GENIChomozygous56960217
4142226641142226642AG31GENIChomozygous56960218
4142227146142227147AG28GENIChomozygous56960219
4142227316142227317TC30GENIChomozygous56960221
4142227353142227354AG32GENIChomozygous56960222
4142227559142227560CG28GENIChomozygous56960223
4142228173142228174CG28GENIChomozygous56960224
4142229679142229680GC21GENIChomozygous56960225
4142229813142229814TC37GENIChomozygous56960226
4142230306142230320TTTTTTTTTTTTTT--------------28GENIChomozygous56960227
4142232649142232650TC21GENIChomozygous57942287
4142233365142233366CG26GENIChomozygous56960228
4142233645142233646GGGTGTGT19GENICheterozygous58467183
4142233645142233646GGGTGTGTGT19GENICheterozygous58341727
4142236002142236004TT--25GENICheterozygous58589464
4142240257142240258GGGA6GENICheterozygous57504217
4142240257142240258GGGAGA6GENICheterozygous58467185
4142242107142242108C-22GENIChomozygous56960233
4142242297142242302ATCCT-----37GENIChomozygous57942290
4142243117142243118TTG14GENIChomozygous56960234
4142236003142236004T-25GENICpossibly homozygous58283698