chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--20INTERGENIChomozygous54262599
7140489834140489835TTA23INTERGENIChomozygous54860752
7140490259140490260TG39INTERGENIChomozygous54262608
7140490283140490284CCATACACACACATACACACACACAGTGGCTGGGATCCACATCTGGACTACACAT30INTERGENIChomozygous54924496
7140490391140490392AAAC21INTERGENIChomozygous54154649
7140490531140490532CT30INTERGENIChomozygous54262618
7140490541140490542TC32INTERGENIChomozygous54262621
7140491223140491224GA37INTERGENIChomozygous54262627
7140491614140491615GA31INTERGENIChomozygous54262630
7140491664140491665GC19INTERGENIChomozygous54262633
7140492521140492522AC34INTERGENIChomozygous54262636
7140493266140493267TC34INTERGENIChomozygous54262638
7140493791140493792TG29INTERGENIChomozygous54262641
7140494070140494071AG26INTERGENIChomozygous54262644
7140494670140494671GA4GENIChomozygous54262647
7140494768140494769A-4GENIChomozygous54262650
7140498070140498071GA28GENIChomozygous54262661
7140498400140498401AAC10GENIChomozygous54262664
7140498584140498585CT28GENIChomozygous54262667
7140498840140498841GA28GENIChomozygous54262670
7140499036140499037GA33GENIChomozygous54262673
7140499201140499202GA22GENIChomozygous54262676
7140499462140499463GA26GENIChomozygous54262679
7140499491140499492CT37GENIChomozygous54262682
7140499532140499533GT34GENIChomozygous54262685
7140502448140502458TGTGTGTGTG----------12INTERGENICpossibly homozygous55016562
7140503494140503495AG23INTERGENIChomozygous54154655
7140504383140504384GGGTGTGTGTGTGTGTGT11INTERGENICheterozygous55016564
7140504383140504384GGGTGTGTGTGTGTGTGTGT11INTERGENICheterozygous55016566