chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 12052883 12052884 G A 21 GENIC homozygous 602657381 20 12052919 12052920 G A 16 GENIC homozygous 602657382 20 12053347 12053348 C CCA 43 GENIC possibly homozygous 730675381 20 12053805 12053806 G A 16 GENIC homozygous 601946815 20 12053859 12053860 C CCAGGCCCTCGG 4 GENIC homozygous 730675382 20 12054006 12054007 C T 13 GENIC homozygous 601946816 20 12054013 12054014 A G 16 GENIC homozygous 601946817 20 12054034 12054035 C T 19 GENIC homozygous 601946818 20 12054130 12054131 C T 24 GENIC homozygous 602657383 20 12054644 12054645 G C 28 GENIC homozygous 601946819 20 12054707 12054708 G T 24 GENIC homozygous 601946820 20 12055259 12055260 A AGG 15 GENIC possibly homozygous 730675383 20 12055338 12055339 T G 19 GENIC homozygous 601946821 20 12055480 12055481 G A 14 GENIC homozygous 602657384 20 12055481 12055482 T C 13 GENIC homozygous 602657385 20 12055509 12055510 C T 8 GENIC homozygous 602657386