chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 140887210 140887211 T G 37 GENIC homozygous 940853035 4 140887405 140887406 G C 28 GENIC homozygous 940853036 4 140887526 140887527 A G 19 GENIC homozygous 940853037 4 140887695 140887696 G A 25 GENIC homozygous 940853038 4 140888161 140888162 G T 19 GENIC homozygous 940853039 4 140894149 140894150 G A 22 GENIC homozygous 940853040 4 140896988 140896989 G A 32 GENIC homozygous 940853041 4 140897414 140897415 C T 18 GENIC homozygous 940853042 4 140902715 140902716 T C 16 GENIC homozygous 940853043 4 140902957 140902958 A G 22 GENIC homozygous 940853044 4 140903807 140903808 C T 21 GENIC homozygous 940853045 4 140906350 140906351 A G 31 GENIC homozygous 940853046 4 140906395 140906396 A G 40 GENIC homozygous 940853047 4 140908274 140908275 T G 19 GENIC homozygous 940853048 4 140908798 140908799 A G 40 GENIC homozygous 940853049 4 140908994 140908995 G C 15 GENIC homozygous 940853050 4 140909196 140909197 C T 30 GENIC homozygous 940853051 4 140909244 140909245 G T 25 GENIC homozygous 940853052 4 140909248 140909249 T A 25 GENIC homozygous 940853053 4 140916630 140916631 T G 21 GENIC homozygous 940853054 4 140916631 140916632 C A 20 GENIC homozygous 940853055 4 140916796 140916797 C G 22 GENIC homozygous 940853056