chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
82300168123001683AC--32GENICpossibly homozygous761061598
82300205023002051G-22GENICpossibly homozygous761061599
82300210223002103CCT21GENIChomozygous761061600
82300235723002358TC24GENICpossibly homozygous656739905
82300271623002720GTAG----14GENIChomozygous761061601
82300274923002750TTTGTG17GENICheterozygous761061603
82300274923002750TTTGTGTG17GENICheterozygous761061604
82300310423003105GC24GENIChomozygous656739906
82300321923003220CCTGTGTGTG10GENIChomozygous761061608
82300343623003437TC24GENIChomozygous656739907
82300364223003643GA30GENIChomozygous656739908
82300560623005617CAAAAACAAAA-----------21GENIChomozygous761061609
82300609923006100AC36GENIChomozygous656739909
82300661523006617CA--27GENIChomozygous761061610
82300683123006832GGAA9GENIChomozygous761061613
82300722523007226AG32GENICpossibly homozygous656739910
82300751223007513AAAAGAAAGGAAGG20GENICpossibly homozygous761061614
82300778523007786TTAAAAAGTTCGGGGCTGGGGATATAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTTGGTCCCCAGCTCCGAAAAAAAGAACCCCCC21GENIChomozygous761061616
82300781923007821GT--2GENIChomozygous761061617
82300816323008164AG20GENIChomozygous656739911
82300822023008221GT24GENICpossibly homozygous656739912
82300865923008660AAT11GENIChomozygous761061618
82301036123010362AC29GENIChomozygous656739913
82301065023010651CCGTGTGTGTGT4GENIChomozygous761061623
82301164923011650AG21GENIChomozygous656739914
82301172923011730GA16GENIChomozygous656739915
82301189523011896CCAAAA3GENIChomozygous761061625
82301192023011921CCA2GENIChomozygous761061626
82301192323011924CCAAA14GENIChomozygous761061627
82301216823012169TC29GENIChomozygous656739916
82301226523012266CT25GENIChomozygous656739917
82301279223012793TTGTGTGTGTGTGCGTGCGTTGTGC9GENIChomozygous761061628
82301351323013514TG31GENIChomozygous656739918