chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182388445723884457TTCT48GENIChomozygous140215833
182388591123885912TA59GENIChomozygous140286899
182388719323887194AG56GENIChomozygous140286900
182388739323887394GA46GENIChomozygous140286901
182388838923888390CT60GENIChomozygous140286902
182388918423889185TC58GENIChomozygous140286903
182389075223890753TG40GENIChomozygous140286904
182389215723892158GA51GENIChomozygous140286905
182389217723892178CT54GENIChomozygous140286906
182389367523893676AG53GENIChomozygous140286907
182389411123894112CG58GENICpossibly homozygous140286908
182389472523894726CT35GENIChomozygous140286909
182389481923894827GCTGCTCT50GENIChomozygous140215834
182389482723894828TA52GENIChomozygous140286910
182389498523894986AG51GENIChomozygous140286911
182389672023896721TC55GENIChomozygous140286912
182389874223898743CT44GENIChomozygous140286913
182389879823898799GA45GENIChomozygous140286914
182389892723898928GA30GENIChomozygous140286915
182389906523899066AG12GENICheterozygous403861719
182389906523899066A12GENIChomozygous403861718
182389905623899057GA12GENIChomozygous403861716
182389905623899057G12GENICheterozygous403861717
182389922523899226TG29GENICheterozygous140286916
182389949923899500TA45GENIChomozygous140286917
182390325523903256GA60GENIChomozygous140286918
182390369223903693GA51GENIChomozygous140286919
182390388323903884CT47GENIChomozygous140286920
182390684423906845TC41GENIChomozygous140286921
182390967323909674CT49GENIChomozygous140286922
182390983623909837GA35GENIChomozygous140286923
182391001723910018GT42GENIChomozygous140286924
182391022723910228CA39GENIChomozygous140286925
182391087023910870CTGCCTCTGCCT40GENIChomozygous140215835
182391100223911002CTGCCTCTC31GENIChomozygous140215836
182391256323912564G31GENIChomozygous140215837
182391349823913498C24GENIChomozygous140215838
182391387223913872CA29GENICpossibly homozygous140215839