chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	51620378	51620379	C	CTT	16	GENIC	homozygous	61413150
1	51621149	51621150	G	A	34	GENIC	homozygous	61413152
1	51621521	51621522	A	G	19	GENIC	homozygous	61413153
1	51621613	51621614	T	C	25	GENIC	homozygous	61413154
1	51622054	51622055	A	G	15	GENIC	homozygous	61413155
1	51622355	51622356	G	A	22	GENIC	homozygous	61413156
1	51622498	51622499	C	T	22	GENIC	homozygous	61413157
1	51622517	51622518	C	T	21	GENIC	homozygous	61413158
1	51622518	51622519	T	TC	20	GENIC	homozygous	61413159
1	51622720	51622721	T	C	24	GENIC	homozygous	61413160
1	51622766	51622767	A	ACTCC	32	GENIC	homozygous	61413161