chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	196607156	196607157	A	G	21	GENIC	homozygous	110196087
2	196607918	196607918		A	13	GENIC	homozygous	127722639
2	196607942	196607943	C		15	GENIC	homozygous	127722640
2	196607950	196607950		C	17	GENIC	homozygous	127722641
2	196607960	196607960		T	16	GENIC	homozygous	127722642
2	196607964	196607964		C	16	GENIC	homozygous	127722643
2	196607970	196607970		A	15	GENIC	homozygous	127722644
2	196608048	196608049	A		22	GENIC	homozygous	127722645
2	196608054	196608054		A	22	GENIC	homozygous	127722646
2	196608093	196608094	T		2	GENIC	homozygous	127722647
2	196609411	196609412	T	C	15	GENIC	homozygous	110196089
2	196612473	196612477	TCTG		13	GENIC	homozygous	127722648
2	196619074	196619075	C	T	17	GENIC	homozygous	110196090
2	196623438	196623439	G	A	8	GENIC	homozygous	110196091
2	196643866	196643867	C	T	18	GENIC	homozygous	110196094
2	196648282	196648283	G	A	21	GENIC	homozygous	110196095
2	196648600	196648603	TGA		13	GENIC	possibly homozygous	127722653
2	196651443	196651444	G	A	3	GENIC	homozygous	110196096
2	196622991	196622991		T	12	GENIC	heterozygous	131811251
2	196627276	196627277	C	T	2	GENIC	homozygous	127831289
2	196628341	196628342	C	T	4	GENIC	homozygous	127831290