chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 144054669 144054670 G A 14 GENIC homozygous 126328986 5 144054997 144054998 A G 18 GENIC homozygous 126328988 5 144055644 144055645 G A 14 GENIC homozygous 126328990 5 144055686 144055687 A G 15 GENIC homozygous 126328992 5 144055794 144055795 G A 11 GENIC homozygous 126328994 5 144056229 144056230 G A 20 GENIC homozygous 126328996 5 144056342 144056343 G A 22 GENIC homozygous 114036416 5 144056467 144056468 G T 12 GENIC homozygous 126328998 5 144056520 144056521 G A 20 GENIC homozygous 126329000 5 144056728 144056729 G A 22 GENIC homozygous 126329001 5 144056778 144056779 C A 22 GENIC homozygous 114036418 5 144057053 144057054 G A 9 GENIC homozygous 114036419 5 144057228 144057229 G T 14 GENIC homozygous 126329003 5 144057780 144057781 C T 16 GENIC homozygous 114036420 5 144058606 144058607 A C 17 GENIC homozygous 114036423 5 144059081 144059082 T C 21 GENIC homozygous 126329005 5 144060166 144060167 T A 18 GENIC homozygous 114036424 5 144060808 144060809 G A 5 GENIC heterozygous 122409101 5 144062190 144062191 T A 4 GENIC homozygous 126329007 5 144063866 144063867 G A 8 GENIC homozygous 114152099 5 144060676 144060677 A C 26 GENIC homozygous 114152094 5 144062103 144062104 C T 14 GENIC homozygous 114152097 5 144063894 144063895 C T 16 GENIC homozygous 114152100 5 144064561 144064562 T C 11 GENIC homozygous 114036428 5 144064794 144064795 A G 18 GENIC homozygous 114036429 5 144064944 144064945 T C 6 GENIC homozygous 114036430