chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	73182892	73182893	G	T	15	GENIC	homozygous	121004622
1	73182896	73182896		T	14	GENIC	homozygous	127394260
1	73209239	73209240	C		11	GENIC	homozygous	127394262
1	73209246	73209246		C	11	GENIC	homozygous	127394263
1	73209259	73209260	A		9	GENIC	homozygous	127394264
1	73209263	73209267	ATGC		9	GENIC	homozygous	127394265
1	73209289	73209290	T		5	GENIC	homozygous	127394266
1	73209301	73209301		A	3	GENIC	homozygous	127394267
1	73209308	73209310	GC		1	GENIC	homozygous	127394268
1	73216680	73216682	CT		8	GENIC	homozygous	127394269
1	73216770	73216771	C		7	GENIC	homozygous	127394270
1	73216797	73216798	C		6	GENIC	homozygous	127394271
1	73216873	73216873		C	10	GENIC	homozygous	127394272
1	73217006	73217006		T	1	GENIC	homozygous	127394273
1	73209293	73209294	C	T	5	GENIC	homozygous	127540776
1	73209306	73209307	T	A	1	GENIC	homozygous	127540777
1	73209236	73209237	G	A	11	GENIC	homozygous	108133429