chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 52572157 52572158 G A 5 GENIC homozygous 671469081 9 52572237 52572238 T C 32 GENIC homozygous 671469082 9 52572854 52572855 G T 17 GENIC possibly homozygous 671469083 9 52572903 52572904 A G 14 GENIC homozygous 671469084 9 52572917 52572918 G T 18 GENIC homozygous 671469085 9 52573120 52573121 A G 6 GENIC homozygous 671469086 9 52573178 52573179 T C 6 GENIC heterozygous 671469087 9 52573208 52573209 A T 15 GENIC homozygous 671469088 9 52573234 52573235 C A 18 GENIC homozygous 671469089 9 52573340 52573341 T A 22 GENIC possibly homozygous 671469090 9 52573627 52573628 A G 18 GENIC homozygous 671469091 9 52573730 52573733 TAG --- 4 GENIC homozygous 769045422 9 52573789 52573790 T A 6 GENIC heterozygous 671469092 9 52574192 52574193 A G 29 GENIC possibly homozygous 671469093 9 52574475 52574476 G A 5 GENIC heterozygous 671469094 9 52574489 52574490 C T 6 GENIC homozygous 671469095 9 52574696 52574697 T C 16 GENIC homozygous 671469096 9 52574737 52574738 T C 8 GENIC homozygous 671469097 9 52575120 52575121 G A 19 GENIC homozygous 671469098 9 52575450 52575451 A G 13 GENIC possibly homozygous 671469099 9 52575671 52575672 A G 8 GENIC homozygous 671469100 9 52576268 52576269 C A 18 GENIC heterozygous 671469101 9 52576280 52576281 T G 10 GENIC homozygous 671469102 9 52576321 52576322 G C 15 GENIC homozygous 671469103 9 52576513 52576514 C CT 13 GENIC homozygous 769045423 9 52576610 52576611 T C 16 GENIC homozygous 671469104 9 52576650 52576651 T A 20 GENIC homozygous 671469105 9 52576831 52576832 A G 23 GENIC possibly homozygous 671469106 9 52577012 52577013 A T 25 GENIC homozygous 671469107 9 52577413 52577414 C T 18 GENIC homozygous 671469108 9 52577502 52577503 A T 13 GENIC homozygous 671469109 9 52577622 52577623 A G 9 GENIC homozygous 671469110 9 52577656 52577657 A G 20 GENIC homozygous 671469111