chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--16INTERGENICpossibly homozygous54262599
7140489637140489638C-16INTERGENICheterozygous54154644
7140490259140490260TG21INTERGENICpossibly homozygous54262608
7140490283140490284CCATACACACACATACACACACACAGTGGCTGGGATCCACATCTGGACTACACAT22INTERGENICpossibly homozygous54924496
7140490391140490392AAAC3INTERGENICheterozygous54154649
7140491614140491615GA3INTERGENIChomozygous54262630
7140491664140491665GC14INTERGENICpossibly homozygous54262633
7140492521140492522AC25INTERGENIChomozygous54262636
7140493266140493267TC20INTERGENIChomozygous54262638
7140493791140493792TG12INTERGENICheterozygous54262641
7140494070140494071AG5INTERGENICheterozygous54262644
7140498070140498071GA22GENICheterozygous54262661
7140498400140498401AAC6GENICheterozygous54262664
7140498584140498585CT26GENICpossibly homozygous54262667
7140498840140498841GA23GENICpossibly homozygous54262670
7140499036140499037GA29GENICpossibly homozygous54262673
7140499201140499202GA4GENIChomozygous54262676
7140499462140499463GA17GENIChomozygous54262679
7140499491140499492CT17GENICpossibly homozygous54262682
7140499532140499533GT7GENICheterozygous54262685
7140503494140503495AG8INTERGENICheterozygous54154655