chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140489636140489638CC--8INTERGENIChomozygous54262599
7140490259140490260TG20INTERGENICheterozygous54262608
7140490391140490392AAAC5INTERGENICheterozygous54154649
7140490531140490532CT3INTERGENIChomozygous54262618
7140490541140490542TC2INTERGENIChomozygous54262621
7140491223140491224GA3INTERGENIChomozygous54262627
7140491614140491615GA2INTERGENIChomozygous54262630
7140491664140491665GC6INTERGENIChomozygous54262633
7140492521140492522AC10INTERGENIChomozygous54262636
7140493266140493267TC9INTERGENIChomozygous54262638
7140493791140493792TG8INTERGENICpossibly homozygous54262641
7140494070140494071AG1INTERGENIChomozygous54262644
7140498070140498071GA10GENIChomozygous54262661
7140498584140498585CT14GENICpossibly homozygous54262667
7140498840140498841GA14GENICpossibly homozygous54262670
7140499036140499037GA12GENICpossibly homozygous54262673
7140499201140499202GA6GENICheterozygous54262676
7140499462140499463GA14GENIChomozygous54262679
7140499491140499492CT9GENIChomozygous54262682
7140499532140499533GT4GENICheterozygous54262685
7140503494140503495AG4INTERGENIChomozygous54154655
7140490283140490284CCATACACACACATACACACACACAGTGGCTGGGATCCACATCTGGACTACACAT13INTERGENICpossibly homozygous54924496