chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140511976140511977TA4GENICheterozygous126602972
7140512525140512526AG18GENIChomozygous115938761
7140512576140512577CT21GENIChomozygous115938762
7140513201140513202GC30GENIChomozygous115938763
7140513524140513525TG22GENIChomozygous115938764
7140513827140513828AG22GENIChomozygous115938765
7140513876140513877TC4GENICheterozygous115938766
7140514951140514952AG4GENIChomozygous115938775
7140518099140518100GT21GENIChomozygous115938777
7140518406140518407TC14GENIChomozygous115938779
7140518492140518493GA11GENIChomozygous115938780
7140519422140519423AG11GENIChomozygous115938781
7140521465140521466GA13GENIChomozygous115938782
7140523450140523451CT16GENIChomozygous115938783
7140523491140523492AG19GENIChomozygous115938784
7140523822140523823CT12GENIChomozygous115938785
7140524823140524824TC19GENIChomozygous115938786
7140525155140525156CT11GENIChomozygous115938787
7140525411140525412CT12GENIChomozygous115938788
7140526833140526834CT6GENICheterozygous126602973
7140531892140531893TC10GENIChomozygous115938789
7140535860140535861AG5GENIChomozygous115938793
7140532894140532895AG21GENIChomozygous115938790
7140532966140532967AG14GENIChomozygous115938791
7140534753140534754GA17GENIChomozygous115938792
7140536730140536731CT16GENIChomozygous115938794
7140541089140541090CT15GENICheterozygous115938797
7140541143140541144GA11GENIChomozygous115938798