chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	52380920	52380922	TT		30	GENIC	homozygous	132804530
2	52380928	52380929	T		27	GENIC	homozygous	130863305
2	52380929	52380930	A	G	27	GENIC	homozygous	120141862
2	52381079	52381079		T	34	GENIC	homozygous	131600799
2	52381080	52381081	A	G	34	GENIC	homozygous	120141863
2	52381109	52381110	A	G	42	GENIC	homozygous	110696298
2	52383858	52383859	C	T	54	GENIC	homozygous	110932457
2	52380932	52380933	A	T	26	GENIC	homozygous	110522235
2	52383582	52383583	A	G	57	GENIC	homozygous	110522243
2	52384087	52384088	G		46	GENIC	homozygous	132012786
2	52386683	52386684	A	C	42	GENIC	homozygous	110932458
2	52387259	52387260	T	C	50	GENIC	homozygous	110522268
2	52392900	52392901	C	T	55	GENIC	homozygous	110932459
2	52392988	52392989	T	C	53	GENIC	homozygous	110522298
2	52393966	52393967	G	C	52	GENIC	homozygous	110522306
2	52394261	52394262	A	T	61	GENIC	homozygous	110932460
2	52394821	52394822	G	A	50	GENIC	homozygous	110522310
2	52395617	52395618	A	G	45	GENIC	homozygous	110522312
2	52398759	52398760	C	G	42	GENIC	homozygous	110522325
2	52399248	52399249	G	A	62	GENIC	homozygous	110522327
2	52400389	52400390	G	T	52	GENIC	homozygous	110932461