chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162064738920647390GGTC45GENIChomozygous689825172
162064936620649367C-10GENIChomozygous689825173
162064980820649809GGAAA11GENIChomozygous689825174
162065031820650319GT17GENIChomozygous517790187
162065037020650371TG5GENIChomozygous517790188
162065037220650373TA5GENIChomozygous517790189
162065037920650380CG6GENIChomozygous517790190
162065038720650388AT7GENIChomozygous517790191
162065042820650429TG6GENIChomozygous517790192
162065044020650441CA7GENIChomozygous517790193
162065045120650452CG7GENIChomozygous517790194
162065045720650458TG6GENIChomozygous517790195
162065046020650461AG5GENIChomozygous517790196
162065047020650471CT4GENIChomozygous517790197
162065047920650480CA4GENIChomozygous517790198
162065048820650489TG3GENIChomozygous517790199
162065076520650766TC15GENIChomozygous517790200
162065125520651256TA44GENIChomozygous517790201
162065179520651796CG32GENIChomozygous517790202
162065232520652326CG42GENIChomozygous517790203
162065252420652525TC46GENIChomozygous517790204
162065505220655053GA25GENIChomozygous517790205
162065703520657036TA32GENIChomozygous517790206
162065713820657139GA30GENIChomozygous517790207
162065719420657195TC36GENIChomozygous517790208
162065748720657488CT48GENIChomozygous517790209