chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155029744155029745CG27GENIChomozygous56131215
5155029951155029952TC32GENIChomozygous56238041
5155030634155030635AT24GENIChomozygous56131220
5155030905155030906TC33GENIChomozygous56131221
5155031551155031552AG28GENIChomozygous56131222
5155031605155031606TC28GENIChomozygous56131226
5155031732155031733GA27GENIChomozygous56131227
5155034774155034775CT41GENICpossibly homozygous56238042
5155034995155034996CCA7GENICheterozygous56495172
5155036437155036438GA35GENIChomozygous56238043
5155036777155036778AG28GENIChomozygous56238044
5155038850155038851A-11GENIChomozygous55803824
5155039309155039310C-5GENICheterozygous56751970
5155039868155039869TC46GENIChomozygous56131253
5155041896155041897CT33GENIChomozygous56238045
5155042774155042775AG51GENIChomozygous56131259
5155042981155042982TG41GENIChomozygous56238046
5155043287155043288AG32GENIChomozygous56131260
5155043331155043332TC33GENIChomozygous56238047
5155043610155043611GA24GENIChomozygous56238048
5155043660155043661GT21GENIChomozygous56131262
5155044562155044563T-13GENICheterozygous55803825
5155045228155045229GGA23GENICheterozygous57113337