chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	51620379	51620380	T	-	24	GENIC	homozygous	61868311
1	51620412	51620413	G	A	30	GENIC	homozygous	61868312
1	51620434	51620435	T	A	26	GENIC	homozygous	61868313
1	51620609	51620610	T	C	32	GENIC	homozygous	61868315
1	51620800	51620801	G	GT	26	GENIC	possibly homozygous	61868316
1	51621613	51621614	T	C	42	GENIC	homozygous	61413154
1	51621955	51621956	T	TA	30	GENIC	possibly homozygous	61868317
1	51622054	51622055	A	G	42	GENIC	homozygous	61413155
1	51622152	51622153	C	G	37	GENIC	homozygous	61868318
1	51622498	51622499	C	T	29	GENIC	homozygous	61413157
1	51622720	51622721	T	C	26	GENIC	homozygous	61413160
1	51622766	51622767	A	ACTCC	24	GENIC	homozygous	61413161