chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79151898691518987TC24GENIChomozygous115760115
79151902491519025GA24GENIChomozygous116050554
79152073491520735AG17GENIChomozygous116050556
79152383491523835CT17GENIChomozygous116050558
79152445591524456AG27GENIChomozygous115760121
79152663591526636AG22GENIChomozygous115760125
79152772991527730TC18GENIChomozygous116050560
79152873891528739A23GENIChomozygous128493300
79152898091528980T22GENIChomozygous128493301
79153373591533736TC24GENIChomozygous115760143
79153390191533902TC29GENIChomozygous115760145
79153455591534555TAGTGTATAAGCAAACCTAGCGAAT20GENIChomozygous128493303
79153556691535567AG24GENIChomozygous115760151
79153636791536368CG20GENIChomozygous116050564
79153671791536718CT35GENIChomozygous116050566
79153788491537885CA18GENIChomozygous116050568
79153797991537980AG22GENIChomozygous116050570
79153799291537993CT21GENIChomozygous116050573
79153817991538180TC21GENIChomozygous116050575
79153854891538549GA10GENIChomozygous116050577
79153501491535014A18GENIChomozygous131020981
79153604491536044A22GENIChomozygous131020982
79153680391536803CTC22GENIChomozygous131020983
79153780991537809A25GENIChomozygous131020984