chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 91206966 91206967 C T 13 GENIC homozygous 882702909 3 91207854 91207855 A G 13 GENIC homozygous 882702910 3 91207888 91207889 T G 18 GENIC homozygous 882702911 3 91208211 91208212 G A 13 GENIC homozygous 882702912 3 91208274 91208275 T C 12 GENIC homozygous 882702913 3 91208366 91208367 T C 15 GENIC homozygous 882702914 3 91208897 91208898 A G 4 GENIC heterozygous 882702915 3 91208898 91208899 G T 4 GENIC heterozygous 882702916 3 91208899 91208900 T A 4 GENIC homozygous 882702917 3 91208938 91208939 G A 12 GENIC homozygous 882702918 3 91208961 91208962 A G 14 GENIC homozygous 882702919 3 91209026 91209027 A C 14 GENIC homozygous 882702920 3 91209172 91209173 A G 21 GENIC homozygous 882702921 3 91209557 91209558 A G 32 GENIC homozygous 882702922 3 91209950 91209951 C T 21 GENIC homozygous 882702923 3 91210148 91210149 C T 25 GENIC homozygous 882702924 3 91210943 91210944 T G 28 GENIC homozygous 882702925 3 91211310 91211311 A G 27 GENIC homozygous 882702926 3 91211824 91211825 G C 19 GENIC homozygous 882702927 3 91213023 91213024 C A 8 GENIC homozygous 882702928 3 91213078 91213079 T C 9 GENIC homozygous 882702929 3 91213347 91213348 A G 11 GENIC homozygous 882702930 3 91213418 91213419 C T 17 GENIC homozygous 882702931 3 91215339 91215340 G A 19 GENIC homozygous 882702932