chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 12052883 12052884 G A 20 GENIC homozygous 574518761 20 12052919 12052920 G A 27 GENIC homozygous 574518762 20 12053347 12053348 C CCA 44 GENIC heterozygous 713883658 20 12053350 12053352 CA -- 44 GENIC heterozygous 713883657 20 12053805 12053806 G A 28 GENIC homozygous 573898012 20 12053859 12053860 C CCAGGCCCTCGG 33 GENIC homozygous 713883659 20 12054006 12054007 C T 27 GENIC homozygous 573898013 20 12054013 12054014 A G 30 GENIC homozygous 573898014 20 12054034 12054035 C T 32 GENIC homozygous 573898015 20 12054130 12054131 C T 17 GENIC homozygous 574518763 20 12054644 12054645 G C 36 GENIC homozygous 573898016 20 12054707 12054708 G T 30 GENIC homozygous 573898017 20 12055259 12055260 A AGG 21 GENIC possibly homozygous 713883660 20 12055338 12055339 T G 27 GENIC homozygous 573898018 20 12055480 12055481 G A 33 GENIC homozygous 574518764 20 12055481 12055482 T C 33 GENIC homozygous 574518765 20 12055509 12055510 C T 30 GENIC homozygous 574518766