chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	144135183	144135184	T	C	16	GENIC	homozygous	59873130
2	144135279	144135280	T	C	14	GENIC	homozygous	59873131
2	144135336	144135337	G	A	10	GENIC	homozygous	59873132
2	144135342	144135343	C	CGTGT	6	GENIC	homozygous	59873133
2	144135391	144135392	G	A	22	GENIC	heterozygous	59873134
2	144135444	144135445	A	G	19	GENIC	homozygous	59873135
2	144135462	144135463	A	G	11	GENIC	homozygous	59873136
2	144135465	144135466	A	G	11	GENIC	homozygous	59873137
2	144135572	144135573	T	A	22	GENIC	homozygous	59873138
2	144135865	144135866	G	C	22	GENIC	homozygous	59873139
2	144135869	144135870	A	G	20	GENIC	homozygous	59873140
2	144136093	144136094	A	G	20	GENIC	heterozygous	59873141
2	144136108	144136109	C	T	14	GENIC	homozygous	59873142
2	144136127	144136128	A	G	17	GENIC	homozygous	59873143
2	144136222	144136223	C	T	9	GENIC	possibly homozygous	59873144
2	144136314	144136315	C	A	18	GENIC	possibly homozygous	59873145
2	144136315	144136316	C	T	19	GENIC	possibly homozygous	59873146
2	144136534	144136535	G	C	23	GENIC	heterozygous	59873147
2	144136767	144136768	T	C	33	GENIC	homozygous	59873148
2	144136882	144136883	C	-	19	GENIC	homozygous	59873149
2	144136904	144136905	T	TGTG	13	GENIC	homozygous	59873150