chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243578116243578117CT63GENIChomozygous110348082
2243578117243578118AG63GENICpossibly homozygous110348084
2243578241243578242AG74GENIChomozygous110348086
2243578365243578366AG71GENICpossibly homozygous110348088
2243578698243578699TC78GENIChomozygous110348090
2243581211243581212TC22GENICpossibly homozygous110348092
2243584291243584292AC249GENICheterozygous110633273
2243584411243584412GC246GENICheterozygous110633275
2243584442243584443TC247GENICheterozygous110633277
2243584531243584532CT178GENICheterozygous110633279
2243584900243584901TC191GENICheterozygous110633281
2243587206243587207TA126GENICheterozygous110633283
2243587209243587210AC131GENICheterozygous110348096
2243587371243587372CA52GENICheterozygous110348098
2243587451243587452CA74GENICheterozygous110348100
2243587505243587506TA100GENICheterozygous110633285
2243587733243587734AG61GENIChomozygous110348102
2243589148243589149GA47GENICpossibly homozygous110348107
2243589273243589274AC49GENIChomozygous110348109
2243591982243591983CT59GENIChomozygous110348111
2243592629243592630CG61GENIChomozygous110348113
2243593340243593341GA43GENIChomozygous110348115
2243593358243593359TG47GENIChomozygous110348117
2243594317243594318TC51GENIChomozygous110348119
2243595511243595512GA44GENIChomozygous110348121
2243598435243598436CT67GENIChomozygous110348123
2243599330243599331GA54GENIChomozygous110348125