chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7111047658111047659CT39GENIChomozygous143365670
7111047699111047700AC49GENIChomozygous143365671
7111047721111047722AG54GENIChomozygous143365672
7111048322111048323TC57GENIChomozygous143365673
7111050406111050407GA61GENIChomozygous143365675
7111050503111050504GA51GENIChomozygous143365676
7111050920111050921TA25GENIChomozygous148022115
7111049809111049810TG43GENIChomozygous148022112
7111050545111050546AG49GENIChomozygous148022113
7111050716111050717CT45GENIChomozygous148022114
7111050938111050954GCCCGCCTGCCTGCCT14GENIChomozygous148016044
7111051313111051314CT36GENIChomozygous148022116
7111055168111055169CG45GENIChomozygous143365678
7111054908111054909AT58GENIChomozygous138182046
7111055651111055652CT67GENIChomozygous138182047
7111054908111054908C59GENIChomozygous137974257
7111059293111059294CT10GENIChomozygous148022117
7111059318111059334CCATCCACCCATCCAC10GENIChomozygous148016045
7111061639111061640TA46GENIChomozygous138182049
7111062830111062831TC50GENIChomozygous138182051
7111062845111062846GA49GENIChomozygous148022118
7111063920111063921CT47GENIChomozygous148022119
7111068725111068726AC54GENIChomozygous138182053
7111069262111069263AC38GENIChomozygous138182054
7111071200111071201CT54GENIChomozygous148022120
7111071241111071242CT58GENIChomozygous143365696
7111071287111071288CT48GENIChomozygous138182056
7111071678111071679G49GENIChomozygous148016046
7111072265111072270AAAAG42GENIChomozygous148016047
7111074122111074122CCT52GENIChomozygous137974262
7111071820111071821G21GENICpossibly homozygous403617356
7111071820111071821GA21GENICheterozygous154485231
7111073299111073300TC50GENICheterozygous154485233
7111073299111073300T50GENIChomozygous403617357
7111073304111073305G50GENIChomozygous403617358
7111073304111073305GA50GENICheterozygous403617359