chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	150146787	150146788	G	A	15	GENIC	homozygous	125591309
2	150146894	150146895	C	A	23	GENIC	homozygous	125763169
2	150147443	150147447	AGAC		10	GENIC	homozygous	131292537
2	150147524	150147525	A	C	23	GENIC	homozygous	110052673
2	150147619	150147620	C	T	46	GENIC	homozygous	120373455
2	150148032	150148033	G	A	44	GENIC	homozygous	120373456
2	150148375	150148376	T	C	40	GENIC	homozygous	110052676
2	150148490	150148491	T	C	43	GENIC	homozygous	110052677
2	150148518	150148519	G	T	44	GENIC	homozygous	110052678
2	150148638	150148639	T	G	38	GENIC	homozygous	110052679
2	150148701	150148702	G	A	39	GENIC	homozygous	110052680
2	150149714	150149714		A	47	GENIC	homozygous	131292538
2	150150662	150150663	C	A	42	GENIC	homozygous	120373457
2	150152487	150152488	C	T	35	GENIC	homozygous	120373458
2	150153206	150153216	TAAATAATAT		13	GENIC	homozygous	131292540
2	150156772	150156773	G	T	37	GENIC	homozygous	120373460
2	150157208	150157208		T	38	GENIC	homozygous	131292541
2	150148271	150148271		T	44	GENIC	homozygous	127689989
2	150151239	150151240	T		44	GENIC	homozygous	127689990
2	150152521	150152522	A		29	GENIC	homozygous	127689991