chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 86469288 86469289 T A 8 GENIC homozygous 971880920 2 86469347 86469348 A G 10 GENIC homozygous 971880921 2 86470513 86470514 A G 13 GENIC homozygous 971880922 2 86471752 86471753 G A 19 GENIC homozygous 971880923 2 86471928 86471929 A G 18 GENIC homozygous 971880924 2 86472275 86472276 C T 10 GENIC homozygous 971880925 2 86473337 86473338 T C 9 GENIC homozygous 971880926 2 86474473 86474474 A G 12 GENIC homozygous 971880927 2 86474543 86474544 A C 11 GENIC homozygous 971880928 2 86475285 86475286 T G 10 GENIC homozygous 971880929 2 86475760 86475761 G A 11 GENIC homozygous 971880930 2 86476068 86476069 C A 20 GENIC homozygous 971880931 2 86476837 86476838 C G 22 GENIC homozygous 971880932 2 86477331 86477332 T C 11 GENIC homozygous 971880933 2 86477383 86477384 G T 7 GENIC homozygous 971880934 2 86479764 86479765 T C 11 GENIC homozygous 971880935 2 86480065 86480066 G A 23 GENIC homozygous 971880936 2 86481009 86481010 C T 17 GENIC homozygous 971880937 2 86481236 86481237 T G 8 GENIC possibly homozygous 971880938 2 86481663 86481664 G A 8 GENIC homozygous 971880939 2 86531529 86531530 A G 6 GENIC homozygous 971880940 2 86531539 86531540 G A 8 GENIC homozygous 971880941 2 86546866 86546867 G A 5 GENIC homozygous 971880942 2 86558331 86558332 C T 19 GENIC homozygous 971880943 2 86558867 86558868 C T 23 GENIC homozygous 971880944