chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 75434745 75434746 G C 10 GENIC homozygous 933919085 X 75434747 75434748 T A 9 GENIC homozygous 933919086 X 75435273 75435274 A C 11 GENIC homozygous 933919087 X 75436298 75436299 C T 10 GENIC homozygous 933919088 X 75436796 75436797 C T 7 GENIC homozygous 933919089 X 75437619 75437620 A G 9 GENIC homozygous 933919090 X 75438312 75438313 G A 13 GENIC homozygous 933919091 X 75441489 75441490 A C 9 GENIC homozygous 933919092 X 75441921 75441922 T C 6 GENIC homozygous 933919093 X 75442859 75442860 A G 5 GENIC homozygous 933919094 X 75449460 75449461 T A 6 GENIC homozygous 933919095 X 75452969 75452970 C T 13 GENIC homozygous 933919096 X 75453015 75453016 C G 13 GENIC homozygous 933919097 X 75453724 75453725 A C 7 GENIC homozygous 933919098 X 75493556 75493557 C T 9 INTERGENIC homozygous 933919099 X 75512124 75512125 G T 12 INTERGENIC homozygous 933919100