chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	144135336	144135337	G	A	21	GENIC	homozygous	59873132
2	144135342	144135343	C	CGTGT	7	GENIC	heterozygous	59873133
2	144135342	144135343	C	CGTGTGT	7	GENIC	heterozygous	60500796
2	144135391	144135392	G	A	33	GENIC	possibly homozygous	59873134
2	144135444	144135445	A	G	23	GENIC	homozygous	59873135
2	144135462	144135463	A	G	22	GENIC	homozygous	59873136
2	144135465	144135466	A	G	21	GENIC	homozygous	59873137
2	144135572	144135573	T	A	15	GENIC	homozygous	59873138
2	144135865	144135866	G	C	24	GENIC	homozygous	59873139
2	144135869	144135870	A	G	25	GENIC	homozygous	59873140
2	144136093	144136094	A	ACACACACACACACGCACACACG	21	GENIC	possibly homozygous	60500797
2	144136108	144136109	C	T	21	GENIC	possibly homozygous	59873142
2	144136127	144136128	A	G	16	GENIC	homozygous	59873143
2	144136228	144136229	T	TTTTC	5	GENIC	heterozygous	60580561
2	144136314	144136315	C	A	11	GENIC	homozygous	59873145
2	144136315	144136316	C	T	11	GENIC	homozygous	59873146
2	144136526	144136527	T	TAGAC	11	GENIC	homozygous	60451438
2	144136767	144136768	T	C	27	GENIC	homozygous	59873148
2	144136882	144136883	C	-	30	GENIC	homozygous	59873149
2	144136904	144136905	T	TGTG	23	GENIC	possibly homozygous	59873150