chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7111434032111434033TG17GENIChomozygous138182501
7111434899111434900TC27GENIChomozygous142008277
7111435627111435628C10GENIChomozygous137974364
7111435904111435905TG26GENIChomozygous138182503
7111438982111438983AG33GENIChomozygous142008278
7111439117111439118GA33GENIChomozygous142008279
7111439764111439765AG18GENIChomozygous138182505
7111440277111440278TC16GENIChomozygous138182506
7111440484111440485TG20GENIChomozygous138182507
7111440743111440743TGATGA17GENIChomozygous137974365
7111444102111444103CT21GENIChomozygous138182510
7111445066111445067AG15GENIChomozygous138182511
7111445339111445451AAACTCTTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAGAATAAAAAAAAAAAAAAA9GENIChomozygous137974368
7111445686111445687AT28GENIChomozygous138182512
7111445756111445757AT25GENIChomozygous142008280
7111447329111447330AG18GENIChomozygous138182516
7111435888111435889TG27GENICheterozygous154492307
7111435890111435891TG27GENICheterozygous154492308
7111446216111446217TC12GENIChomozygous138182513
7111446223111446224GA13GENIChomozygous138182514
7111446750111446751GA13GENIChomozygous138182515
7111435888111435889T27GENIChomozygous403222447
7111435890111435891T27GENIChomozygous141922627
7111437032111437032A15GENIChomozygous141922628
7111438248111438250AA14GENICpossibly homozygous141922629
7111449453111449454CT23GENIChomozygous138182518
7111452219111452220C15GENIChomozygous137974369
7111452287111452288CT13GENIChomozygous138182519