chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172483472324834724AG19GENIChomozygous111180972
172483571724835718AG24GENIChomozygous111003042
172483616324836164GA29GENIChomozygous111180974
172483634324836344CT26GENIChomozygous111180976
172483640324836404GC7GENIChomozygous111180978
172483883624838837TA16GENIChomozygous111003046
172484664524846646TG19GENIChomozygous111003048
172484680524846806GA10GENIChomozygous111180988
172484711724847118AG19GENIChomozygous111180990
172484714824847149CA9GENIChomozygous119333912
172484719724847198TC13GENIChomozygous111180992
172484729624847297CT17GENIChomozygous111180994
172484874324848744AC17GENIChomozygous111180996
172484898124848982GT16GENIChomozygous111180998
172484916624849167CT14GENIChomozygous111181000
172485006224850063GA13GENIChomozygous111181002
172485146524851466GA15GENIChomozygous111003052
172485305124853052AG13GENIChomozygous111003054
172485419224854193TC14GENIChomozygous111181008
172485431924854320CA14GENIChomozygous111181010
172485476524854766CT13GENIChomozygous111181012
172485595224855953CT23GENIChomozygous111181014
172485640024856401TC14GENIChomozygous111003068
172485706924857070TG13GENIChomozygous111181016
172485714224857143GA29GENIChomozygous119333916
172485726624857267TC5GENICheterozygous119333922
172485741524857416TA11GENIChomozygous111181018
172485761124857612GC6GENIChomozygous111003072
172485809024858091AG17GENIChomozygous111181020
172486130024861301TC19GENIChomozygous111003084
172485280224852803GA5GENIChomozygous125546176
172485741324857414CA5GENIChomozygous125546177