chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 91212378 91212379 T TGC 16 GENIC heterozygous 51539277 10 91212383 91212385 GC -- 16 GENIC possibly homozygous 51539278 10 91212866 91212867 C A 18 GENIC homozygous 51539279 10 91215806 91215807 C - 17 GENIC heterozygous 51539280 10 91215848 91215858 GTGTGTGTGT ---------- 8 GENIC heterozygous 51539281 10 91216360 91216361 G A 39 GENIC homozygous 51539282 10 91216712 91216713 C T 50 GENIC homozygous 51539283 10 91219687 91219688 G T 61 GENIC homozygous 51539284 10 91219794 91219795 C G 53 GENIC homozygous 51539285 10 91220682 91220683 G A 40 GENIC homozygous 51539286 10 91220753 91220754 A T 49 GENIC homozygous 51539287 10 91221084 91221085 G A 29 GENIC possibly homozygous 51539288 10 91221218 91221226 CTTTTTTT -------- 11 GENIC homozygous 51539289 10 91221219 91221223 TTTT ---- 13 GENIC possibly homozygous 51539290 10 91221263 91221264 C G 28 GENIC possibly homozygous 51539291 10 91221389 91221390 T G 42 GENIC heterozygous 51539292 10 91221477 91221478 C G 49 GENIC homozygous 51539293 10 91221580 91221581 C T 28 GENIC homozygous 51539294 10 91221634 91221635 A G 37 GENIC homozygous 51539295 10 91222132 91222133 G A 51 GENIC possibly homozygous 51539296