chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 93983009 93983010 G A 37 GENIC homozygous 51745915 10 93984387 93984388 T TC 4 GENIC homozygous 51745917 10 93984539 93984540 G T 15 GENIC homozygous 51745919 10 93984905 93984906 C A 21 GENIC homozygous 51745921 10 93986802 93986803 A C 22 GENIC homozygous 51745923 10 93990522 93990523 G A 24 GENIC homozygous 51745925 10 93991439 93991440 G A 32 GENIC possibly homozygous 51547910 10 93993106 93993107 A G 21 GENIC homozygous 51745927 10 93993150 93993151 G C 24 GENIC homozygous 51745929 10 93993388 93993389 C T 19 GENIC homozygous 51547914 10 93993419 93993420 C T 11 GENIC homozygous 51745931 10 93993547 93993548 C CTTTTT 7 GENIC homozygous 52398947 10 93993693 93993694 A G 24 GENIC homozygous 51547915 10 93994217 93994218 T TC 41 GENIC homozygous 51547917 10 93994873 93994874 T TA 6 GENIC heterozygous 52167359 10 93995913 93995914 C T 24 GENIC homozygous 51745933 10 93997035 93997036 G GAC 19 GENIC homozygous 51547925 10 93998649 93998650 C T 26 GENIC homozygous 51745935 10 93999785 93999786 G A 31 GENIC homozygous 51745937 10 94000280 94000281 C T 19 GENIC homozygous 51745939 10 94001690 94001691 T C 34 GENIC homozygous 51547931 10 94002094 94002095 T C 31 GENIC homozygous 51547932 10 94002200 94002201 A G 27 GENIC homozygous 51547933 10 94004374 94004375 C T 26 GENIC homozygous 51745941