chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	196602497	196602497		TGTGTGTGTA	6	GENIC	heterozygous	127722638
2	196607156	196607157	A	G	49	GENIC	possibly homozygous	110196087
2	196607918	196607918		A	34	GENIC	homozygous	127722639
2	196607942	196607943	C		36	GENIC	homozygous	127722640
2	196607950	196607950		C	38	GENIC	homozygous	127722641
2	196607960	196607960		T	39	GENIC	homozygous	127722642
2	196607964	196607964		C	39	GENIC	homozygous	127722643
2	196607970	196607970		A	35	GENIC	homozygous	127722644
2	196608048	196608049	A		35	GENIC	homozygous	127722645
2	196608054	196608054		A	32	GENIC	homozygous	127722646
2	196608093	196608094	T		4	GENIC	homozygous	127722647
2	196609411	196609412	T	C	31	GENIC	homozygous	110196089
2	196612473	196612477	TCTG		39	GENIC	possibly homozygous	127722648
2	196619074	196619075	C	T	48	GENIC	homozygous	110196090
2	196623438	196623439	G	A	44	GENIC	homozygous	110196091
2	196639841	196639841		A	7	GENIC	homozygous	127722650
2	196639858	196639859	G		10	GENIC	homozygous	127722651
2	196639872	196639872		G	10	GENIC	homozygous	127722652
2	196643866	196643867	C	T	53	GENIC	homozygous	110196094
2	196648282	196648283	G	A	63	GENIC	homozygous	110196095
2	196648600	196648603	TGA		38	GENIC	homozygous	127722653
2	196651443	196651444	G	A	10	GENIC	homozygous	110196096
2	196627276	196627277	C	T	4	GENIC	homozygous	127831289
2	196628341	196628342	C	T	15	GENIC	homozygous	127831290