chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130792381130792382TA8GENIChomozygous116726308
8130793203130793204TC13GENIChomozygous116726309
8130793751130793752AG27GENIChomozygous116726310
8130795224130795225AG23GENIChomozygous116726311
8130797414130797415AG7GENIChomozygous116726312
8130797535130797536CT14GENIChomozygous116726313
8130798279130798280GA9GENIChomozygous116726314
8130799449130799450TC18GENIChomozygous116726315
8130799774130799775AG22GENIChomozygous116726316
8130800259130800260CT27GENIChomozygous116726317
8130800357130800358CT18GENIChomozygous116726318
8130800463130800464TC19GENIChomozygous116726319
8130800588130800589GA7GENIChomozygous116726320
8130801687130801688GA9GENIChomozygous116726321
8130802081130802082CG11GENICheterozygous126702027
8130802231130802232GA17GENIChomozygous116726323
8130803938130803939CT18GENIChomozygous116726327