chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 158429117 158429118 C T 49 GENIC homozygous 149035917 5 158429198 158429199 A G 45 GENIC homozygous 149035918 5 158429305 158429306 A G 45 GENIC homozygous 145560528 5 158429398 158429399 G A 46 GENIC homozygous 149035919 5 158429434 158429435 G A 40 GENIC homozygous 149035920 5 158429476 158429477 A G 46 GENIC homozygous 149035921 5 158429500 158429501 A C 46 GENIC possibly homozygous 149035922 5 158429516 158429517 G A 47 GENIC homozygous 149035923 5 158429692 158429693 C T 38 GENIC homozygous 149035924 5 158429727 158429728 C T 41 GENIC homozygous 149035925 5 158429929 158429930 C T 47 GENIC homozygous 149035926 5 158429955 158429956 A C 38 GENIC homozygous 149035927 5 158429962 158429963 C T 36 GENIC homozygous 149035928 5 158429963 158429964 A G 36 GENIC homozygous 145560531 5 158429985 158429986 G C 37 GENIC homozygous 149035929 5 158430259 158430260 C T 36 GENIC homozygous 149035930 5 158430261 158430262 T C 35 GENIC homozygous 149035931