chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	143926493	143926494	A	C	35	GENIC	homozygous	59872599
2	143926838	143926839	A	T	29	GENIC	homozygous	59872600
2	143927892	143927893	G	A	19	GENIC	homozygous	59872601
2	143928339	143928340	C	CGT	10	GENIC	possibly homozygous	61398081
2	143928514	143928515	A	C	28	GENIC	homozygous	59872602
2	143929169	143929170	A	G	29	GENIC	homozygous	59872603
2	143929258	143929259	C	T	40	GENIC	homozygous	59872604
2	143930178	143930179	T	A	31	GENIC	homozygous	59872605
2	143930321	143930326	GGGCT	-----	37	GENIC	homozygous	59872606
2	143931474	143931475	T	C	28	GENIC	homozygous	59872607
2	143931825	143931826	G	A	30	GENIC	homozygous	59872608
2	143932047	143932048	C	T	35	GENIC	homozygous	59872609