chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 120387249 120387250 G A 14 GENIC homozygous 54084081 7 120387941 120387942 T C 7 GENIC homozygous 54084082 7 120389509 120389510 C T 10 GENIC heterozygous 54084084 7 120389607 120389608 A G 13 GENIC homozygous 54084085 7 120389713 120389714 A G 17 GENIC homozygous 54084086 7 120390296 120390297 A G 25 GENIC possibly homozygous 54084087 7 120390388 120390389 G C 15 GENIC possibly homozygous 54084089 7 120390927 120390928 T C 3 GENIC homozygous 54084091 7 120391170 120391171 A G 9 GENIC possibly homozygous 54084092 7 120391780 120391781 A G 25 GENIC homozygous 54084093 7 120392222 120392223 G A 19 GENIC possibly homozygous 54084094 7 120392936 120392937 G A 21 GENIC homozygous 54234171 7 120393749 120393750 T C 15 GENIC possibly homozygous 54084096 7 120394797 120394798 T C 6 GENIC heterozygous 54084098 7 120394923 120394924 T C 4 GENIC heterozygous 54084099 7 120394944 120394945 T G 4 GENIC heterozygous 54084100 7 120395441 120395442 T C 3 GENIC homozygous 54084101 7 120396585 120396586 T TC 2 GENIC heterozygous 54234175