chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5148910340148910341CG2GENIChomozygous55786181
5148911064148911065AT2GENICheterozygous55786183
5148911066148911067TC2GENICheterozygous55786185
5148915260148915270CTGATTCCTT----------5GENIChomozygous55786195
5148916254148916255TC20GENICpossibly homozygous55786197
5148916619148916622ATC---5GENIChomozygous55786199
5148916892148916893GT1GENIChomozygous55786201
5148917284148917285AG6GENIChomozygous55786203
5148919848148919849TC7GENIChomozygous55786219
5148921496148921497CT15GENIChomozygous55786227
5148922475148922476CCT3GENICheterozygous56532552
5148922995148922996CA11GENICheterozygous55786229
5148923349148923350CCAT3GENIChomozygous55786231
5148925729148925730TG14GENIChomozygous55786233
5148927175148927176AG13GENICpossibly homozygous55786235
5148927643148927644TA1GENIChomozygous56355969
5148928324148928325A-17GENICheterozygous55786239
5148930211148930212GGTGGGTTGTTGT3GENIChomozygous55786247
5148930419148930420AAC21GENIChomozygous55786253
5148931383148931384T-18GENIChomozygous55786255
5148931874148931875AAC6GENIChomozygous56355970
5148932006148932007AAAAC3GENIChomozygous55786259
5148934513148934514TTG6GENICheterozygous56355971
5148934514148934515TTGTGTGTG6GENICheterozygous56355972
5148937726148937727AG8GENICpossibly homozygous55786277
5148940373148940374CCAT5GENIChomozygous55786279
5148942196148942197GT7GENIChomozygous55786281
5148944621148944622CT3GENICheterozygous55786283
5148945168148945169CT10GENIChomozygous55786285
5148948289148948290TTGTGTG3GENIChomozygous55786295
5148948291148948292TG3GENIChomozygous56355973
5148948295148948296TG3GENIChomozygous55786301
5148948297148948298TG3GENIChomozygous55786303
5148953139148953140TC18GENICpossibly homozygous55786309
5148953729148953852TGGAAACGGTAGGAAAGGGACTTCTGTAACCGCTCTTTACGTGGAAACGGTAGGAAAGGGACTTCTGTAACCGCTCTTTACGTGGAAACGGTAGGAAAGGGACTTCTGTAACTGCTCTTTACG---------------------------------------------------------------------------------------------------------------------------30GENICheterozygous56355974