chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 91212343 91212351 GTGTGTGT -------- 7 GENIC possibly homozygous 52508753 10 91212866 91212867 C A 15 GENIC homozygous 51539279 10 91215806 91215807 C - 17 GENIC homozygous 51539280 10 91215848 91215858 GTGTGTGTGT ---------- 6 GENIC heterozygous 51539281 10 91216360 91216361 G A 40 GENIC homozygous 51539282 10 91216712 91216713 C T 22 GENIC homozygous 51539283 10 91217937 91217938 C - 33 GENIC homozygous 51739178 10 91217964 91217965 C T 36 GENIC homozygous 51739180 10 91218114 91218115 G - 22 INTERGENIC possibly homozygous 51739182 10 91218146 91218150 TCTT ---- 33 INTERGENIC homozygous 52166059 10 91213234 91213235 C G 32 GENIC homozygous 52166056 10 91216982 91216983 G C 14 GENIC homozygous 52166057 10 91217757 91217758 A G 22 GENIC homozygous 52166058 10 91219687 91219688 G T 14 GENIC homozygous 51539284 10 91219758 91219759 A ATCTGAGGCC 20 GENIC homozygous 52166060 10 91220289 91220290 G A 31 GENIC homozygous 52166061 10 91220452 91220453 A G 31 GENIC homozygous 51739188 10 91220714 91220715 T C 28 GENIC homozygous 52166062 10 91220753 91220754 A T 30 GENIC homozygous 51539287 10 91221084 91221085 G A 33 GENIC homozygous 51539288 10 91221218 91221226 CTTTTTTT -------- 27 GENIC homozygous 51539289 10 91221294 91221295 C T 18 GENIC homozygous 52166063 10 91221477 91221478 C G 25 GENIC homozygous 51539293 10 91221580 91221581 C T 26 GENIC homozygous 51539294 10 91221634 91221635 A G 41 GENIC homozygous 51539295 10 91222132 91222133 G A 28 GENIC homozygous 51539296