chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 126364514 126364515 T C 16 GENIC heterozygous 147265021 7 126431412 126431413 C T 7 GENIC heterozygous 147265022 7 126431413 126431414 G A 7 GENIC heterozygous 147265023 7 126439086 126439087 G A 11 GENIC homozygous 403226014 7 126439086 126439087 G 11 GENIC heterozygous 403226015 7 126445676 126445677 G A 44 GENIC possibly homozygous 147265024 7 126472702 126472703 T C 22 GENIC heterozygous 141013150 7 126472700 126472701 T C 18 GENIC heterozygous 141013149 7 126483800 126483801 G A 15 GENIC heterozygous 154487949 7 126483800 126483801 G 15 GENIC heterozygous 403226041 7 126504856 126504857 A 8 GENIC heterozygous 403771723 7 126403609 126403613 CTAT 13 GENIC homozygous 141010215 7 126504853 126504857 CTCA 7 GENIC heterozygous 141010216 7 126504856 126504857 A T 8 GENIC heterozygous 403771724 7 126514408 126514409 A C 49 GENIC possibly homozygous 147265025 7 126517771 126517772 G C 28 GENIC heterozygous 154487959 7 126517771 126517772 G 28 GENIC heterozygous 403226046 7 126565110 126565111 T 39 GENIC heterozygous 403226049 7 126565110 126565111 T C 39 GENIC heterozygous 403226050 7 126628262 126628263 G 15 GENIC heterozygous 403618279 7 126628262 126628263 G T 15 GENIC heterozygous 403618280