chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198573021198573022TC16GENIChomozygous108497980
1198573047198573048CT22GENIChomozygous108497982
1198573075198573076TG23GENIChomozygous108497984
1198573211198573212CT6GENIChomozygous108497986
1198573918198573919CT26GENIChomozygous108497988
1198574194198574195CT15GENIChomozygous108497990
1198574499198574500GA18GENIChomozygous108497993
1198574591198574592TC16GENIChomozygous108497995
1198575501198575502CT22GENIChomozygous108497997
1198575659198575660GA9GENIChomozygous108497999
1198577183198577184AC7GENIChomozygous108498001
1198579298198579299TC12GENIChomozygous108498007
1198579305198579306AC13GENIChomozygous108498009
1198579740198579741TC21GENIChomozygous108498011
1198580031198580032CT23GENIChomozygous108498013
1198580742198580743AG12GENIChomozygous108498015
1198580918198580919GA15GENIChomozygous108498017
1198581142198581143GT14GENIChomozygous108498019
1198582842198582843GA26GENIChomozygous108498023
1198582976198582977CT16GENIChomozygous108498025
1198583122198583123GA15GENIChomozygous108498027
1198583806198583807TC12GENIChomozygous108498029
1198583995198583996GA22GENIChomozygous108498031
1198584826198584827AG10GENIChomozygous108498033
1198585578198585579GC21GENIChomozygous108498035