chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 42783543 42783544 T C 16 GENIC homozygous 641790609 9 42783663 42783664 A G 29 GENIC homozygous 641790610 9 42783860 42783861 T TCA 10 GENIC heterozygous 752127895 9 42783860 42783861 T TCACA 10 GENIC heterozygous 752127896 9 42785547 42785548 T C 2 GENIC homozygous 641790611 9 42786198 42786199 A G 43 GENIC homozygous 641790612 9 42786816 42786817 C T 37 GENIC homozygous 641790613 9 42789530 42789531 C T 19 GENIC homozygous 641790614 9 42791343 42791344 T TG 33 GENIC possibly homozygous 752127897 9 42792776 42792777 C G 29 GENIC homozygous 641790615 9 42793083 42793084 T C 26 GENIC homozygous 641790616