chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105613618656136187G-2GENIChomozygous52377665
105613619956136200GC8GENICheterozygous52377667
105613632556136326GA16GENIChomozygous51891104
105613639256136393GA19GENIChomozygous51891106
105613785856137868GTGTGTGTGT----------23GENIChomozygous51891109
105613801256138013AC25GENIChomozygous51654501
105613806956138070A-9GENIChomozygous52377669
105613987456139875TTATAC1GENIChomozygous52377671
105614010556140106GA29GENIChomozygous51891115
105614037556140376C-20GENIChomozygous51459993
105614037756140378CA20GENICpossibly homozygous52377673
105614070856140709CT34GENIChomozygous51891118
105614224556142246T-10GENICheterozygous51891121
105614268056142681TTTGTGTGTGTG15GENIChomozygous52377675
105614410956144110AG34GENIChomozygous51654519
105614425856144259TC33GENIChomozygous51654521
105614436056144362TG--3GENIChomozygous51986691
105614490856144909CT33GENIChomozygous51891125
105614680456146805GT25GENIChomozygous51654525