chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129798708 129798709 C T 7 GENIC homozygous 1000764849 7 129799658 129799659 G A 5 GENIC homozygous 1000764850 7 129800613 129800614 C T 11 GENIC homozygous 1000764851 7 129801117 129801118 A G 10 GENIC homozygous 1000764852 7 129801936 129801937 G A 5 GENIC homozygous 1000764853 7 129804694 129804695 T G 8 GENIC homozygous 1000764854 7 129804776 129804777 T C 6 GENIC homozygous 1000764855 7 129804821 129804822 G A 2 GENIC homozygous 1000764856 7 129805161 129805162 T C 5 GENIC homozygous 1000764857 7 129805282 129805283 A G 11 GENIC homozygous 1000764858 7 129805315 129805316 T C 11 GENIC homozygous 1000764859 7 129805327 129805328 G T 10 GENIC homozygous 1000764860 7 129806589 129806590 C T 5 GENIC homozygous 1000764861 7 129807636 129807637 C A 3 GENIC homozygous 1000764862 7 129808777 129808778 C T 6 GENIC homozygous 1000764863 7 129808911 129808912 G T 8 GENIC homozygous 1000764864 7 129808987 129808988 A G 11 GENIC homozygous 1000764865 7 129810320 129810321 T C 8 GENIC homozygous 1000764866 7 129810349 129810350 T C 11 GENIC homozygous 1000764867 7 129810795 129810796 C T 6 GENIC homozygous 1000764868 7 129810829 129810830 G A 10 GENIC homozygous 1000764869 7 129811223 129811224 A G 2 GENIC homozygous 1000764870