chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--28INTERGENIChomozygous54262599
7140490259140490260TG29INTERGENIChomozygous54262608
7140490391140490392AAAC14INTERGENIChomozygous54154649
7140490531140490532CT7INTERGENIChomozygous54262618
7140490541140490542TC7INTERGENIChomozygous54262621
7140494768140494769A-2GENIChomozygous54262650
7140491223140491224GA5INTERGENIChomozygous54262627
7140491614140491615GA9INTERGENIChomozygous54262630
7140491664140491665GC9INTERGENIChomozygous54262633
7140492521140492522AC25INTERGENIChomozygous54262636
7140493266140493267TC33INTERGENIChomozygous54262638
7140493791140493792TG26INTERGENIChomozygous54262641
7140494070140494071AG22INTERGENIChomozygous54262644
7140490283140490284CCATACACACACATACACACACACAGTGGCTGGGATCCACATCTGGACTACACAT20INTERGENIChomozygous54924496
7140498070140498071GA30GENIChomozygous54262661
7140498400140498401AAC13GENICheterozygous54262664
7140498584140498585CT20GENIChomozygous54262667
7140498840140498841GA33GENIChomozygous54262670
7140499036140499037GA42GENIChomozygous54262673
7140499201140499202GA31GENIChomozygous54262676
7140499462140499463GA44GENICpossibly homozygous54262679
7140499491140499492CT48GENICpossibly homozygous54262682
7140499532140499533GT44GENIChomozygous54262685
7140503494140503495AG28INTERGENIChomozygous54154655
7140502448140502458TGTGTGTGTG----------7INTERGENIChomozygous55016562
7140504383140504384GGGTGTGTGTGTGTGTGT4INTERGENICheterozygous55016564
7140504383140504384GGGTGTGTGTGTGTGTGTGT4INTERGENICheterozygous55016566