chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7111434032111434033TG43GENIChomozygous138182501
7111434899111434900TC57GENIChomozygous142008277
7111435627111435628C42GENIChomozygous137974364
7111435890111435891T59GENIChomozygous141922627
7111435904111435905TG59GENIChomozygous138182503
7111437032111437032A46GENIChomozygous141922628
7111438248111438250AA48GENIChomozygous141922629
7111438982111438983AG58GENIChomozygous142008278
7111439117111439118GA50GENIChomozygous142008279
7111439764111439765AG45GENIChomozygous138182505
7111440277111440278TC44GENIChomozygous138182506
7111440484111440485TG54GENIChomozygous138182507
7111440743111440743TGATGA30GENIChomozygous137974365
7111444102111444103CT50GENIChomozygous138182510
7111445066111445067AG50GENIChomozygous138182511
7111445339111445451AAACTCTTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAGAATAAAAAAAAAAAAAAA15GENIChomozygous137974368
7111445686111445687AT44GENIChomozygous138182512
7111445756111445757AT47GENIChomozygous142008280
7111446216111446217TC39GENIChomozygous138182513
7111446223111446224GA38GENIChomozygous138182514
7111446750111446751GA30GENIChomozygous138182515
7111447329111447330AG50GENIChomozygous138182516
7111449453111449454CT55GENICpossibly homozygous138182518
7111452219111452220C39GENIChomozygous137974369
7111452287111452288CT37GENIChomozygous138182519
7111435890111435891TG59GENICheterozygous154492308
7111435888111435889T59GENIChomozygous403222447
7111435888111435889TG59GENICheterozygous154492307