chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--11INTERGENICheterozygous54262599
7140489637140489638C-11INTERGENICheterozygous54154644
7140490259140490260TG11INTERGENICpossibly homozygous54262608
7140491664140491665GC5INTERGENIChomozygous54262633
7140492521140492522AC15INTERGENIChomozygous54262636
7140493266140493267TC16INTERGENIChomozygous54262638
7140493791140493792TG4INTERGENIChomozygous54262641
7140494070140494071AG2INTERGENICheterozygous54262644
7140498070140498071GA15GENIChomozygous54262661
7140498584140498585CT21GENICpossibly homozygous54262667
7140498840140498841GA16GENIChomozygous54262670
7140499201140499202GA2GENIChomozygous54262676
7140499532140499533GT2GENIChomozygous54262685
7140490283140490284CCATACACACACATACACACACACAGTGGCTGGGATCCACATCTGGACTACACAT8INTERGENICpossibly homozygous54924496
7140491995140491996TG15INTERGENIChomozygous55960491
7140499399140499400GC17GENIChomozygous55960492
7140501575140501576CT16INTERGENICpossibly homozygous55960493