chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105974965159749652AG54GENIChomozygous116608663
105974994159749942GA75GENIChomozygous116608665
105975011659750117AG64GENIChomozygous116608667
105975081659750817CT51GENIChomozygous116608669
105975124959751249AAG41GENIChomozygous128820910
105975135659751363CTGAACT62GENIChomozygous128820911
105975197259751973TC66GENIChomozygous116608671
105975253259752533C63GENIChomozygous128820912
105975253359752534CG64GENIChomozygous116608673
105975487959754880AG66GENIChomozygous116608675
105975589659755897TA56GENIChomozygous116608677
105975670859756720AGGGAGGGAGGG53GENIChomozygous128820913
105975744359757444TC61GENIChomozygous116608679
105975870259758703GA56GENIChomozygous116608681
105975891859758919AG70GENIChomozygous116608683
105975894759758948AG63GENIChomozygous116608685
105976014659760147TC57GENIChomozygous116788954
105976041359760414AT56GENIChomozygous116608691
105976065059760651GC70GENIChomozygous116608693
105976114659761150CTGT57GENIChomozygous128820914
105976129359761294AG74GENIChomozygous116788955
105976138459761385TC63GENIChomozygous117995656
105976138959761390CG60GENIChomozygous117995657
105976139359761393T58GENIChomozygous128820915
105976143359761434GA52GENIChomozygous117995658
105976189559761896GT77GENIChomozygous116608695
105976326559763266GA65GENIChomozygous116608697
105976341159763412TC60GENIChomozygous116608699
105976356859763568G57GENIChomozygous128820916
105976595159765951T56GENIChomozygous128820917
105977058359770584CA69GENIChomozygous116608701
105977063959770640CA61GENIChomozygous116608703
105977144059771441TC55GENIChomozygous116608705
105976791159767912AC11GENICheterozygous132333207