chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157382773157382774GC26GENIChomozygous112906055
4157388743157388744TG16GENIChomozygous112906057
4157392261157392262GA17GENIChomozygous112906067
4157394855157394856AG20GENIChomozygous112906069
4157394856157394857AG20GENIChomozygous112906071
4157396167157396168GA13GENIChomozygous112906073
4157397875157397876CT22GENIChomozygous112906075
4157399492157399493TC13GENIChomozygous112906077
4157399850157399851CA20GENIChomozygous112906079
4157400365157400366GA20GENIChomozygous112906081
4157400388157400389CA24GENIChomozygous112906083
4157400419157400420TC22GENIChomozygous112906085
4157402357157402358AG13GENIChomozygous112906093
4157403131157403132TA27GENIChomozygous112906095
4157403947157403948TC21GENIChomozygous112906097
4157404786157404787CG28GENIChomozygous112906099
4157405666157405667GA18GENIChomozygous112906101
4157407511157407512AC22GENIChomozygous112906103
4157407709157407710CT15GENIChomozygous112906105
4157408171157408172CT35GENIChomozygous112906107