chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	52147760	52147761	A	G	16	GENIC	homozygous	112650860
4	52147937	52147938	A	G	12	GENIC	homozygous	112650861
4	52148185	52148186	A	T	15	GENIC	homozygous	112650862
4	52148198	52148199	T	A	12	GENIC	homozygous	112650863
4	52150709	52150710	A	T	13	GENIC	homozygous	113233199
4	52152802	52152803	C	T	34	GENIC	homozygous	112650864
4	52153123	52153124	A	C	25	GENIC	homozygous	112650865
4	52153227	52153228	T	C	18	GENIC	homozygous	112650866
4	52153266	52153267	C	T	15	GENIC	homozygous	112650867
4	52154803	52154804	C	G	17	GENIC	homozygous	112650869
4	52155193	52155194	G	A	11	GENIC	possibly homozygous	112650870
4	52156356	52156357	T	C	21	GENIC	homozygous	112650871
4	52156738	52156739	G	A	17	GENIC	homozygous	112650872
4	52157505	52157506	G	A	28	GENIC	homozygous	112650873
4	52157771	52157772	T	A	8	GENIC	homozygous	112650874
4	52157915	52157916	T	C	14	GENIC	homozygous	112650875
4	52159741	52159742	G	A	16	GENIC	homozygous	112650876
4	52159791	52159792	T	C	21	GENIC	homozygous	112650877
4	52160338	52160339	C	T	29	GENIC	homozygous	112650878
4	52162658	52162659	T	G	15	GENIC	homozygous	112650879
4	52163741	52163742	T	C	13	GENIC	possibly homozygous	112650880
4	52165026	52165027	A	G	15	GENIC	homozygous	112650881
4	52165101	52165102	C	T	25	GENIC	homozygous	112650882
4	52165111	52165112	G	T	22	GENIC	homozygous	112650883
4	52165909	52165910	A	C	13	GENIC	homozygous	112650884