chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141552576141552580AGGA----11GENICpossibly homozygous54159247
7141553181141553182CT33GENIChomozygous54159248
7141553795141553796AG26GENIChomozygous54159262
7141554086141554087GA25GENIChomozygous54159264
7141554803141554804GGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA12GENIChomozygous55017148
7141554984141554985AG27GENIChomozygous54159265
7141556759141556761GA--41GENIChomozygous54159267
7141553701141553704AAA---10GENICheterozygous55100369
7141553705141553732GAAAGGAAAGGAAAGGAAAGGAAAGGA---------------------------13GENICheterozygous55100371
7141554544141554545AAAGTAGT12GENIChomozygous55100373
7141556415141556416TTACAC13GENICheterozygous55100375
7141556415141556416TTACACAC13GENICheterozygous55100377
7141558254141558255CCT34GENIChomozygous54159268
7141558885141558886AG46GENIChomozygous54159269
7141559005141559006A-25GENICpossibly homozygous54159270
7141561513141561514CT40GENIChomozygous54159271
7141561731141561732AAG16GENICpossibly homozygous54159272
7141561731141561732AAAG16GENICheterozygous54159273
7141561935141561936A-17GENICpossibly homozygous54267124
7141562182141562183T-28GENIChomozygous54159274
7141562828141562829TC48GENIChomozygous54159275
7141563927141563928AG53GENIChomozygous54159276