chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	42353840	42353841	C	T	45	GENIC	homozygous	143578403
13	42354470	42354472	AA		40	GENIC	possibly homozygous	144924565
13	42354521	42354522	T	C	41	GENIC	homozygous	143578405
13	42354839	42354840	C	T	46	GENIC	homozygous	143578406
13	42355616	42355617	A	G	40	GENIC	homozygous	143578407
13	42355895	42355896	A	G	60	GENIC	homozygous	143578408
13	42357204	42357205	G	A	43	GENIC	homozygous	144929029
13	42356154	42356155	G	A	51	GENIC	homozygous	144929025
13	42356660	42356661	G	A	35	GENIC	homozygous	144929026
13	42356845	42356846	G	A	56	GENIC	homozygous	144929027
13	42356999	42357000	G	C	38	GENIC	homozygous	144929028
13	42357224	42357225	C	T	39	GENIC	homozygous	144929030
13	42357315	42357316	C	T	33	GENIC	homozygous	144929031
13	42357329	42357330	T	C	31	GENIC	homozygous	144929032
13	42357354	42357355	T	C	41	GENIC	homozygous	144929033
13	42357607	42357608	C	A	38	GENIC	homozygous	144929034
13	42357765	42357766	G	A	29	GENIC	homozygous	144929035
13	42357776	42357777	A	G	34	GENIC	homozygous	144929036
13	42357795	42357796	A	G	39	GENIC	homozygous	144929037
13	42357831	42357832	G	A	46	GENIC	homozygous	144929038
13	42358123	42358124	T	C	50	GENIC	homozygous	144929039
13	42358243	42358244	C	T	49	GENIC	homozygous	144929040
13	42358336	42358337	T	C	47	GENIC	homozygous	144929041
13	42358403	42358404	G	A	44	GENIC	homozygous	144929042