chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 49394442 49394443 A AGT 7 GENIC heterozygous 758112622 3 49407074 49407078 TAGA ---- 9 GENIC homozygous 758112625 3 49409555 49409556 G GTTTGGTTTGGTTTGGTTTGGTTTGGTTTGGTTT 13 GENIC heterozygous 758112628 3 49409557 49409558 C CTT 18 GENIC heterozygous 758112630 3 49409559 49409560 C CATTTTTTTTTT 15 GENIC heterozygous 758112632 3 49409560 49409561 C CAAG 16 GENIC heterozygous 758112633 3 49409755 49409756 C - 16 GENIC homozygous 758112634 3 49411355 49411356 G GT 22 GENIC homozygous 758112635 3 49411369 49411370 C CT 23 GENIC homozygous 758112636 3 49416593 49416594 T A 30 GENIC homozygous 651771358 3 49419558 49419559 G A 10 GENIC homozygous 651771359 3 49419562 49419563 G A 9 GENIC homozygous 651771360 3 49419575 49419576 T A 10 GENIC homozygous 651771361 3 49419949 49419950 A - 7 GENIC homozygous 758112637 3 49420673 49420683 GTGTGTGTGT ---------- 2 GENIC heterozygous 758112639 3 49421974 49421975 T - 10 GENIC heterozygous 758112641 3 49422176 49422177 T TAGATTGC 11 GENIC homozygous 758112642 3 49422180 49422181 A ATTT 11 GENIC homozygous 758112643 3 49422181 49422182 G GGCAAACTAT 11 GENIC homozygous 758112644 3 49424939 49424940 A AGGGCCTT 17 GENIC homozygous 758112645 3 49429880 49429882 TG -- 2 GENIC heterozygous 758112647 3 49441470 49441471 C CCCTATCTGCAAAGAAGAAAAGGTAGGAG 3 GENIC homozygous 758112648 3 49441473 49441474 G GGAGCTGATGAGTGGGAGGTGAACTTCTTAAATCCGTAATTAAAAAAAATACTTCTAAAAATACAAT 3 GENIC homozygous 758112649 3 49445917 49445919 TG -- 5 GENIC heterozygous 758112652 3 49447759 49447760 C CTAT 4 GENIC homozygous 758112655 3 49458586 49458587 T TA 8 GENIC heterozygous 758112656 3 49458586 49458587 T TAA 8 GENIC heterozygous 758112657 3 49461849 49461850 A - 11 GENIC heterozygous 758112658 3 49462609 49462610 T G 4 GENIC homozygous 651771362