chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	243821978	243821978		TTG	43	GENIC	homozygous	127757243
2	243822070	243822072	AA		47	GENIC	homozygous	132810644
2	243822074	243822075	A	C	48	GENIC	homozygous	120247587
2	243822653	243822653		TTGTTCA	53	GENIC	homozygous	127757244
2	243823686	243823687	C	T	43	GENIC	homozygous	110349755
2	243824219	243824219		T	38	GENIC	heterozygous	129871152
2	243827856	243827856		A	42	GENIC	homozygous	127757245
2	243828219	243828219		T	30	GENIC	homozygous	132810645
2	243828634	243828635	A	G	35	GENIC	homozygous	120162253
2	243828827	243828828	G	A	44	GENIC	possibly homozygous	110349761
2	243829876	243829877	C	T	38	GENIC	homozygous	120247588
2	243830546	243830547	T	A	37	GENIC	homozygous	110349765
2	243830566	243830568	GG		34	GENIC	homozygous	132810646
2	243831469	243831470	A	C	51	GENIC	homozygous	110349769
2	243832865	243832865		G	32	GENIC	homozygous	127757246
2	243832882	243832883	A	G	36	GENIC	homozygous	110349773
2	243834734	243834735	T	C	47	GENIC	homozygous	120247589
2	243835941	243835942	G	A	45	GENIC	homozygous	120247590
2	243836327	243836328	G	A	48	GENIC	homozygous	120247591
2	243838413	243838417	ATAA		34	GENIC	homozygous	132810647
2	243838872	243838873	G	A	44	GENIC	homozygous	110349790
2	243840407	243840408	T		31	GENIC	homozygous	127757248
2	243840592	243840593	T	A	53	GENIC	homozygous	110349794
2	243840819	243840819		TACGCTTTACTCTTGACT	22	GENIC	homozygous	132810648
2	243841888	243841889	G	C	37	GENIC	homozygous	110349796
2	243843205	243843206	C	T	39	GENIC	homozygous	120247593
2	243847375	243847376	G	A	43	GENIC	homozygous	132820005
2	243849267	243849268	G	A	50	GENIC	homozygous	120247594
2	243853676	243853677	G	A	42	GENIC	homozygous	120247595
2	243843368	243843373	TTTTG		38	GENIC	homozygous	132810649