chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	207437429	207437430	C	T	41	GENIC	homozygous	110907534
2	207437752	207437754	GA		44	GENIC	homozygous	132019205
2	207439071	207439072	G	A	58	GENIC	homozygous	110907535
2	207439263	207439264	A	G	56	GENIC	homozygous	110907536
2	207441152	207441153	C	T	62	GENIC	homozygous	110907538
2	207441727	207441728	A	G	64	GENIC	homozygous	110217055
2	207441821	207441822	T	C	60	GENIC	homozygous	110907539
2	207442076	207442077	C	T	57	GENIC	homozygous	110907540
2	207443691	207443692	T	C	44	GENIC	homozygous	110907542
2	207444147	207444148	A	G	52	GENIC	homozygous	110907544
2	207446751	207446752	T	C	61	GENIC	homozygous	110907546
2	207450762	207450763	T		56	GENIC	homozygous	132019214
2	207451232	207451233	A	T	38	GENIC	homozygous	110907551
2	207456551	207456552	A	C	45	GENIC	homozygous	110907552
2	207448437	207448437		GTGC	57	GENIC	possibly homozygous	133082598
2	207440285	207440286	G	A	67	GENIC	homozygous	111161867
2	207456408	207456409	C	A	68	GENIC	possibly homozygous	111161869
2	207447558	207447559	C	T	37	GENIC	homozygous	120215638
2	207447942	207447945	CCT		15	GENIC	homozygous	133082597