chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155029744155029745CG8GENIChomozygous56131215
5155029951155029952TC12GENIChomozygous56238041
5155030634155030635AT18GENIChomozygous56131220
5155030905155030906TC21GENIChomozygous56131221
5155031551155031552AG24GENIChomozygous56131222
5155031605155031606TC14GENIChomozygous56131226
5155031732155031733GA20GENIChomozygous56131227
5155034774155034775CT13GENIChomozygous56238042
5155036437155036438GA16GENIChomozygous56238043
5155036777155036778AG19GENIChomozygous56238044
5155039868155039869TC18GENIChomozygous56131253
5155041896155041897CT16GENIChomozygous56238045
5155042774155042775AG14GENIChomozygous56131259
5155042981155042982TG10GENIChomozygous56238046
5155043287155043288AG15GENIChomozygous56131260
5155043331155043332TC19GENIChomozygous56238047
5155043610155043611GA13GENIChomozygous56238048
5155043660155043661GT10GENIChomozygous56131262