chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 49394442 49394443 A AGT 1 GENIC homozygous 772636466 3 49397339 49397340 G GCA 4 GENIC heterozygous 772636470 3 49407074 49407078 TAGA ---- 3 GENIC homozygous 772636471 3 49409555 49409556 G GTTTGGTTTGGTTTGGTTTGGTTTGGTTTGGTTT 1 GENIC homozygous 772636474 3 49409557 49409558 C CTT 1 GENIC homozygous 772636476 3 49409559 49409560 C CATTTTTTTTTT 1 GENIC homozygous 772636478 3 49409560 49409561 C CAAG 1 GENIC homozygous 772636479 3 49409755 49409756 C - 3 GENIC homozygous 772636480 3 49411355 49411356 G GT 8 GENIC homozygous 772636481 3 49411369 49411370 C CT 9 GENIC homozygous 772636482 3 49416593 49416594 T A 4 GENIC homozygous 677639259 3 49419558 49419559 G A 3 GENIC homozygous 677639260 3 49419562 49419563 G A 3 GENIC homozygous 677639261 3 49419575 49419576 T A 2 GENIC homozygous 677639262 3 49419949 49419950 A - 8 GENIC homozygous 772636483 3 49422176 49422177 T TAGATTGC 7 GENIC homozygous 772636484 3 49422180 49422181 A ATTT 9 GENIC homozygous 772636485 3 49422181 49422182 G GGCAAACTAT 9 GENIC homozygous 772636486 3 49424939 49424940 A AGGGCCTT 7 GENIC homozygous 772636487 3 49428875 49428876 T TA 4 GENIC heterozygous 772636489 3 49429880 49429882 TG -- 5 GENIC heterozygous 772636491 3 49441470 49441471 C CCCTATCTGCAAAGAAGAAAAGGTAGGAG 1 GENIC homozygous 772636492 3 49441473 49441474 G GGAGCTGATGAGTGGGAGGTGAACTTCTTAAATCCGTAATTAAAAAAAATACTTCTAAAAATACAAT 1 GENIC homozygous 772636493 3 49445910 49445911 A ATG 4 GENIC heterozygous 772636497 3 49458586 49458587 T TAA 2 GENIC heterozygous 772636499 3 49462609 49462610 T G 5 GENIC homozygous 677639263