chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116604980766049808GC26GENIChomozygous115886021
116605154966051550CT30GENIChomozygous115886023
116605205066052051AC24GENIChomozygous115886025
116605213666052137GA15GENIChomozygous115886027
116605236666052367GA32GENIChomozygous115886029
116605292866052929CA24GENIChomozygous115886031
116605353066053531CT15GENIChomozygous115886033
116605360766053608AG13GENIChomozygous115886035
116605395866053959AG22GENIChomozygous115886037
116605603566056036GT23GENIChomozygous115886039
116606223266062233CT27GENIChomozygous115886041
116606436066064361CT28GENIChomozygous115886043
116606508566065086CT16GENIChomozygous115886045
116607255766072558CT30GENIChomozygous115886049
116607638966076390TC23GENIChomozygous115886051
116607862166078622TC24GENIChomozygous115886053