chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129798708 129798709 C T 18 GENIC homozygous 950230479 7 129799658 129799659 G A 10 GENIC homozygous 950230480 7 129800613 129800614 C T 16 GENIC homozygous 950230481 7 129801117 129801118 A G 2 GENIC homozygous 950230482 7 129801936 129801937 G A 10 GENIC homozygous 950230483 7 129804694 129804695 T G 15 GENIC homozygous 950230484 7 129804776 129804777 T C 9 GENIC homozygous 950230485 7 129804821 129804822 G A 10 GENIC possibly homozygous 950230486 7 129805161 129805162 T C 14 GENIC homozygous 950230487 7 129805282 129805283 A G 17 GENIC homozygous 950230488 7 129805315 129805316 T C 18 GENIC homozygous 950230489 7 129805327 129805328 G T 17 GENIC homozygous 950230490 7 129806000 129806001 C T 19 GENIC homozygous 950230491 7 129806589 129806590 C T 17 GENIC homozygous 950230492 7 129807333 129807334 G A 7 GENIC homozygous 950230493 7 129807636 129807637 C A 10 GENIC homozygous 950230494 7 129808777 129808778 C T 11 GENIC homozygous 950230495 7 129808911 129808912 G T 13 GENIC homozygous 950230496 7 129808987 129808988 A G 11 GENIC homozygous 950230497 7 129810320 129810321 T C 19 GENIC homozygous 950230498 7 129810349 129810350 T C 20 GENIC homozygous 950230499 7 129810795 129810796 C T 22 GENIC homozygous 950230500 7 129810829 129810830 G A 19 GENIC homozygous 950230501 7 129811223 129811224 A G 23 GENIC homozygous 950230502