chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--18INTERGENIChomozygous54262599
7140490259140490260TG18INTERGENICpossibly homozygous54262608
7140490283140490284CCATACACACACATACACACACACAGTGGCTGGGATCCACATCTGGACTACACAT8INTERGENICpossibly homozygous54924496
7140490391140490392AAAC7INTERGENIChomozygous54154649
7140490531140490532CT5INTERGENIChomozygous54262618
7140490541140490542TC5INTERGENIChomozygous54262621
7140491223140491224GA1INTERGENIChomozygous54262627
7140491614140491615GA12INTERGENIChomozygous54262630
7140491664140491665GC9INTERGENIChomozygous54262633
7140492521140492522AC10INTERGENIChomozygous54262636
7140493266140493267TC22INTERGENIChomozygous54262638
7140493791140493792TG11INTERGENIChomozygous54262641
7140494070140494071AG4INTERGENIChomozygous54262644
7140494768140494769A-2GENIChomozygous54262650
7140498070140498071GA21GENIChomozygous54262661
7140498400140498401AAC4GENIChomozygous54262664
7140498584140498585CT12GENIChomozygous54262667
7140498840140498841GA29GENIChomozygous54262670
7140499036140499037GA19GENICpossibly homozygous54262673
7140499201140499202GA17GENIChomozygous54262676
7140499462140499463GA18GENIChomozygous54262679
7140499491140499492CT22GENIChomozygous54262682
7140499532140499533GT26GENIChomozygous54262685
7140503494140503495AG14INTERGENIChomozygous54154655
7140502448140502458TGTGTGTGTG----------4INTERGENICheterozygous55016562
7140504383140504384GGGTGTGTGTGTGTGTGT6INTERGENICheterozygous55016564
7140504383140504384GGGTGTGTGTGTGTGTGTGT6INTERGENICheterozygous55016566