chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 164041199 164041200 G T 35 GENIC homozygous 111806214 3 164042509 164042510 A C 28 GENIC homozygous 111806216 3 164043898 164043899 G C 33 GENIC homozygous 111806218 3 164044410 164044411 C T 27 GENIC homozygous 111806222 3 164044501 164044502 G A 22 GENIC homozygous 111806224 3 164044511 164044512 C A 26 GENIC homozygous 111806226 3 164045672 164045673 T C 22 GENIC homozygous 111806228 3 164046514 164046515 A G 33 GENIC homozygous 111806230 3 164047970 164047971 A C 22 GENIC homozygous 111806232 3 164049231 164049232 C T 18 GENIC homozygous 111806234 3 164052789 164052790 C A 21 GENIC homozygous 111806236 3 164052859 164052860 G A 20 GENIC homozygous 111806238 3 164052873 164052874 G C 16 GENIC homozygous 111806240 3 164053607 164053608 G T 5 GENIC homozygous 111806246 3 164053614 164053615 G C 3 GENIC homozygous 111806248 3 164053618 164053619 A C 4 GENIC homozygous 111806250 3 164053979 164053980 G C 15 GENIC homozygous 111806252