chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129798708 129798709 C T 34 GENIC homozygous 988411756 7 129799658 129799659 G A 22 GENIC homozygous 988411757 7 129800613 129800614 C T 28 GENIC homozygous 988411758 7 129801117 129801118 A G 21 GENIC homozygous 988411759 7 129801936 129801937 G A 9 GENIC homozygous 988411760 7 129804694 129804695 T G 40 GENIC homozygous 988411761 7 129804776 129804777 T C 35 GENIC homozygous 988411762 7 129804821 129804822 G A 28 GENIC homozygous 988411763 7 129805161 129805162 T C 31 GENIC homozygous 988411764 7 129805282 129805283 A G 19 GENIC homozygous 988411765 7 129805315 129805316 T C 16 GENIC homozygous 988411766 7 129805327 129805328 G T 13 GENIC homozygous 988411767 7 129806000 129806001 C T 38 GENIC homozygous 988411768 7 129806589 129806590 C T 33 GENIC homozygous 988411769 7 129807333 129807334 G A 29 GENIC homozygous 988411770 7 129807636 129807637 C A 8 GENIC homozygous 988411771 7 129808777 129808778 C T 34 GENIC homozygous 988411772 7 129808911 129808912 G T 31 GENIC homozygous 988411773 7 129808987 129808988 A G 33 GENIC homozygous 988411774 7 129810320 129810321 T C 25 GENIC homozygous 988411775 7 129810349 129810350 T C 27 GENIC homozygous 988411776 7 129810795 129810796 C T 24 GENIC homozygous 988411777 7 129810829 129810830 G A 25 GENIC homozygous 988411778 7 129811223 129811224 A G 28 GENIC homozygous 988411779