chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	196607156	196607157	A	G	39	GENIC	homozygous	110196087
2	196607918	196607918		A	25	GENIC	homozygous	127722639
2	196607942	196607943	C		29	GENIC	homozygous	127722640
2	196607950	196607950		C	28	GENIC	homozygous	127722641
2	196607960	196607960		T	28	GENIC	homozygous	127722642
2	196607964	196607964		C	28	GENIC	homozygous	127722643
2	196607970	196607970		A	30	GENIC	homozygous	127722644
2	196608048	196608049	A		27	GENIC	homozygous	127722645
2	196608054	196608054		A	27	GENIC	homozygous	127722646
2	196608093	196608094	T		6	GENIC	homozygous	127722647
2	196609411	196609412	T	C	33	GENIC	homozygous	110196089
2	196612473	196612477	TCTG		23	GENIC	heterozygous	127722648
2	196619074	196619075	C	T	42	GENIC	homozygous	110196090
2	196623438	196623439	G	A	37	GENIC	homozygous	110196091
2	196648600	196648603	TGA		35	GENIC	homozygous	127722653
2	196619948	196619949	T	C	35	GENIC	homozygous	110808041
2	196643866	196643867	C	T	40	GENIC	homozygous	110196094
2	196648282	196648283	G	A	44	GENIC	homozygous	110196095
2	196651443	196651444	G	A	9	GENIC	homozygous	110196096
2	196627276	196627277	C	T	4	GENIC	homozygous	127831289
2	196628341	196628342	C	T	17	GENIC	homozygous	127831290
2	196646659	196646660	T	A	11	GENIC	heterozygous	132578374