chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--13INTERGENIChomozygous54262599
7140490259140490260TG11INTERGENIChomozygous54262608
7140490285140490286CT13INTERGENICheterozygous54262612
7140490313140490314CA10INTERGENICheterozygous54154647
7140490391140490392AAAC7INTERGENIChomozygous54154649
7140491223140491224GA10INTERGENIChomozygous54262627
7140491614140491615GA12INTERGENIChomozygous54262630
7140491664140491665GC15INTERGENIChomozygous54262633
7140492521140492522AC16INTERGENIChomozygous54262636
7140493266140493267TC20INTERGENIChomozygous54262638
7140493791140493792TG19INTERGENIChomozygous54262641
7140494070140494071AG8INTERGENIChomozygous54262644
7140498070140498071GA9GENIChomozygous54262661
7140498584140498585CT14GENIChomozygous54262667
7140498840140498841GA15GENIChomozygous54262670
7140499036140499037GA17GENIChomozygous54262673
7140499201140499202GA12GENIChomozygous54262676
7140499462140499463GA26GENIChomozygous54262679
7140499491140499492CT22GENIChomozygous54262682
7140499532140499533GT20GENIChomozygous54262685
7140503494140503495AG14INTERGENIChomozygous54154655
7140490295140490296CT13INTERGENICheterozygous56444087
7140499230140499231A-14GENICheterozygous56444089