chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 15970092 15970096 ACAC ---- 20 GENIC heterozygous 753501778 20 15970094 15970096 AC -- 20 GENIC possibly homozygous 753501779 20 15970378 15970379 C - 14 GENIC possibly homozygous 753501781 20 15970406 15970414 CTCTCTCT -------- 7 GENIC heterozygous 753501782 20 15970408 15970414 CTCTCT ------ 7 GENIC possibly homozygous 753501783 20 15970462 15970463 T TGCGCGCGCGCGC 14 GENIC possibly homozygous 753501784 20 15970469 15970470 A G 14 GENIC possibly homozygous 644031029 20 15970698 15970699 A G 14 GENIC homozygous 644031030 20 15971118 15971119 C CCACA 22 GENIC homozygous 753501785 20 15971529 15971530 T C 24 GENIC homozygous 644031031 20 15971677 15971678 G A 15 GENIC homozygous 644031032 20 15971693 15971694 C CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 10 GENIC heterozygous 753501786 20 15971705 15971706 A C 3 GENIC homozygous 644031033 20 15971812 15971813 T TTCCAG 13 GENIC homozygous 753501787 20 15971816 15971817 G - 15 GENIC homozygous 753501788 20 15971842 15971843 T C 18 GENIC homozygous 644031034 20 15972036 15972037 C G 25 GENIC homozygous 644031035 20 15972086 15972087 G A 26 GENIC homozygous 644031036 20 15972115 15972116 G A 24 GENIC homozygous 644031037 20 15972164 15972165 G C 27 GENIC homozygous 644031038 20 15972612 15972613 C CTT 28 GENIC homozygous 753501789 20 15972968 15972969 C T 26 GENIC homozygous 644031039 20 15973391 15973392 G C 26 GENIC homozygous 644031040 20 15973699 15973700 A AG 24 GENIC homozygous 753501790 20 15974734 15974735 A G 30 GENIC homozygous 644031041