chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 9708828 9708828 TG 65 GENIC homozygous 129421257 17 9708994 9709104 AAGAATGTTCCAGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAA 53 GENIC possibly homozygous 129421258 17 9709280 9709281 T C 20 GENIC homozygous 125623826 17 9710144 9710144 CA 70 GENIC possibly homozygous 131750602 17 9712829 9712830 A G 65 GENIC homozygous 110952917 17 9712921 9712922 T C 59 GENIC homozygous 110952919 17 9713101 9713102 T C 22 GENIC homozygous 111669334 17 9713514 9713515 C T 64 GENIC homozygous 110952921 17 9716960 9716963 AGG 74 GENIC homozygous 129421260 17 9717778 9717779 A G 93 GENIC homozygous 111524197 17 9718645 9718646 A 49 GENIC possibly homozygous 130706567 17 9719114 9719115 C 65 GENIC homozygous 131750603 17 9720368 9720369 G A 74 GENIC homozygous 110952927