chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118556574118556577TCT---21GENICheterozygous687725045
8118556578118556583TCTGT-----23GENICheterozygous687725047
8118556691118556692GA11GENIChomozygous512659513
8118556845118556846AG17GENIChomozygous512659514
8118557229118557230GGA11GENICheterozygous687725048
8118557231118557232AAACTGAATATCAGGGAT17GENIChomozygous687725049
8118557553118557554GA22GENIChomozygous515300906
8118557615118557617AC--15GENICheterozygous687725050
8118557617118557618A-15GENICheterozygous687725051
8118557618118557620CC--7GENICpossibly homozygous687725052
8118557881118557882AG17GENIChomozygous515300907
8118557936118557937AATT11GENIChomozygous687725053
8118557968118557969AG11GENICpossibly homozygous515300908
8118558134118558135TG13GENICpossibly homozygous512659515
8118558151118558152CT14GENIChomozygous515300909
8118558191118558192AG22GENIChomozygous515300910
8118558202118558203CT23GENICheterozygous515300911
8118558233118558234CG21GENIChomozygous515300912
8118558340118558341AG18GENIChomozygous512659516
8118558364118558365GGC15GENIChomozygous687725054
8118558460118558461TC22GENIChomozygous512659517
8118558497118558498AG24GENIChomozygous512659518
8118558560118558561GGAC24GENIChomozygous687725055
8118558729118558730AG27GENIChomozygous512659519
8118558744118558745CA27GENIChomozygous512659520
8118558831118558832TTTAA1GENIChomozygous687725056
8118558987118558988AC15GENIChomozygous512659521
8118559066118559096TACAGTTAATGTTTACGTTATTTGCACGTA------------------------------9GENIChomozygous687725059
8118559355118559356AG21GENIChomozygous512659522
8118559501118559502TC24GENIChomozygous515300913
8118559559118559560TC23GENIChomozygous515300914
8118559642118559643TG22GENIChomozygous515300915
8118559741118559742TG19GENIChomozygous512659523
8118559823118559824CCATAA3GENIChomozygous687725060
8118559950118559951GA24GENIChomozygous515300916
8118560021118560022CT23GENIChomozygous512659524