chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 42783543 42783544 T C 28 GENIC homozygous 560912166 9 42783663 42783664 A G 24 GENIC homozygous 560912167 9 42783860 42783861 T TCA 12 GENIC heterozygous 707504616 9 42783860 42783861 T TCACA 12 GENIC heterozygous 707504617 9 42785547 42785548 T C 1 GENIC homozygous 560912168 9 42786198 42786199 A G 27 GENIC homozygous 560912169 9 42786816 42786817 C T 28 GENIC homozygous 560912170 9 42789530 42789531 C T 42 GENIC homozygous 560912171 9 42791343 42791344 T TG 20 GENIC possibly homozygous 707504618 9 42792776 42792777 C G 9 GENIC homozygous 560912172 9 42793083 42793084 T C 4 GENIC homozygous 560912173