chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 15969998 15969999 G - 67 GENIC homozygous 696588147 20 15970092 15970094 AC -- 27 GENIC homozygous 696588149 20 15970416 15970417 C T 15 GENIC heterozygous 535487672 20 15970467 15970468 G GCGCGCGCGCGCGCGCGCGCGCACA 7 GENIC homozygous 696588150 20 15970698 15970699 A G 37 GENIC homozygous 535487673 20 15970880 15970893 GCAATCAAGGGAG ------------- 20 GENIC homozygous 696588152 20 15971112 15971113 A ACC 25 GENIC homozygous 696588153 20 15971344 15971345 A G 58 GENIC homozygous 535487674 20 15971529 15971530 T C 35 GENIC homozygous 535487675 20 15971677 15971678 G A 23 GENIC possibly homozygous 535487676 20 15971812 15971813 T TTCCAG 12 GENIC homozygous 696588155 20 15971816 15971817 G - 15 GENIC homozygous 696588156 20 15971842 15971843 T C 24 GENIC homozygous 535487677 20 15972036 15972037 C G 48 GENIC homozygous 535487678 20 15972164 15972165 G C 49 GENIC possibly homozygous 535487679 20 15972478 15972479 C T 40 GENIC homozygous 535487680 20 15972612 15972613 C CTT 42 GENIC homozygous 696588157 20 15972640 15972641 G A 49 GENIC possibly homozygous 535487681 20 15972725 15972726 A C 36 GENIC heterozygous 535487682 20 15972832 15972833 A - 43 GENIC homozygous 696588158 20 15973391 15973392 G C 32 GENIC possibly homozygous 535487683 20 15974734 15974735 A G 36 GENIC homozygous 535487684