chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	160391382	160391383	T	C	39	GENIC	homozygous	111792218
3	160392776	160392777	G	A	50	GENIC	homozygous	111792220
3	160392895	160392896	T	A	52	GENIC	homozygous	111792222
3	160393851	160393851		T	54	GENIC	homozygous	127948341
3	160393818	160393819	C		50	GENIC	homozygous	127948338
3	160393823	160393823		C	51	GENIC	homozygous	127948339
3	160393839	160393839		C	50	GENIC	homozygous	127948340
3	160393860	160393860		C	53	GENIC	homozygous	127948342
3	160393874	160393875	T		59	GENIC	homozygous	127948343
3	160394203	160394204	C	T	57	GENIC	homozygous	111792224
3	160394643	160394643		T	56	GENIC	homozygous	127948344
3	160395742	160395743	T	C	54	GENIC	homozygous	111792226
3	160396164	160396164		TTTTTTCTTTTT	22	GENIC	heterozygous	127948345
3	160396222	160396223	C	T	32	GENIC	homozygous	111792228
3	160396978	160396979	G	A	44	GENIC	homozygous	111792230
3	160397139	160397140	A	T	41	GENIC	homozygous	111792232
3	160397172	160397173	C	T	41	GENIC	homozygous	111792234
3	160397778	160397779	A	G	39	GENIC	homozygous	111792236
3	160399790	160399791	C	G	59	GENIC	homozygous	111792238
3	160399811	160399812	C		69	GENIC	homozygous	127948346
3	160399816	160399817	C	A	66	GENIC	homozygous	119652563
3	160397342	160397343	T	A	2	GENIC	homozygous	130923514
3	160397338	160397339	T	A	2	GENIC	homozygous	130923512
3	160397340	160397341	T	A	2	GENIC	homozygous	130923513