chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 111676152 111676153 T C 27 GENIC homozygous 794734291 8 111676535 111676536 T C 48 GENIC homozygous 794734292 8 111676727 111676728 A C 42 GENIC homozygous 794734293 8 111677564 111677565 T C 35 GENIC homozygous 794734294 8 111677792 111677793 A G 42 GENIC homozygous 794734295 8 111678092 111678093 C T 39 GENIC homozygous 794734296 8 111678149 111678150 A G 41 GENIC homozygous 794734297 8 111678156 111678157 G C 39 GENIC homozygous 794734298 8 111679047 111679048 C G 36 GENIC possibly homozygous 794734299 8 111680019 111680020 T C 45 GENIC homozygous 794734300 8 111680058 111680059 T C 43 GENIC homozygous 794734301 8 111682019 111682020 A G 28 GENIC homozygous 794734302 8 111682251 111682252 A G 32 GENIC heterozygous 794734303 8 111682267 111682268 G A 32 GENIC homozygous 794734304 8 111682438 111682439 A G 36 GENIC homozygous 794734305 8 111683450 111683451 T C 28 GENIC homozygous 794734306 8 111684688 111684689 A G 53 GENIC homozygous 794734307 8 111684944 111684945 G A 42 GENIC homozygous 794734308 8 111685486 111685487 C T 50 GENIC homozygous 794734309 8 111685985 111685986 A G 44 GENIC homozygous 794734310