chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 9758998 9758999 G T 19 GENIC homozygous 109631313 19 9759810 9759811 A G 15 GENIC homozygous 109631315 19 9761651 9761652 T C 24 GENIC homozygous 109631317 19 9761733 9761734 A G 23 GENIC homozygous 109631319 19 9762595 9762596 A G 19 GENIC homozygous 109631321 19 9762650 9762651 A G 21 GENIC homozygous 109631323 19 9763926 9763927 A G 33 GENIC homozygous 109631326 19 9764603 9764604 G C 15 GENIC homozygous 109631328 19 9764828 9764829 T C 20 GENIC homozygous 109631330 19 9759809 9759810 A 15 GENIC homozygous 129582798 19 9761939 9761939 ATGTTGTCATGG 19 GENIC homozygous 129582799 19 9765846 9765847 T 15 GENIC possibly homozygous 129582800 19 9766187 9766188 G A 28 GENIC homozygous 109764355