chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	73564408	73564409	A	G	46	GENIC	homozygous	111859858
16	73565285	73565295	GTGTGTTCTT		44	GENIC	homozygous	133781020
16	73565625	73565626	T	C	41	GENIC	homozygous	111859859
16	73565705	73565706	A	G	48	GENIC	homozygous	111859860
16	73566530	73566531	C	T	38	GENIC	possibly homozygous	111859861
16	73568021	73568022	T	G	45	GENIC	homozygous	111859864
16	73568444	73568445	G	A	40	GENIC	homozygous	111859865
16	73570337	73570338	G	A	51	GENIC	homozygous	111859867
16	73571059	73571060	G	A	49	GENIC	possibly homozygous	111859868
16	73571530	73571531	A	G	54	GENIC	homozygous	111859869
16	73571531	73571532	A	G	54	GENIC	homozygous	111859870
16	73572189	73572190	T	G	55	GENIC	homozygous	111859872
16	73572499	73572500	C	T	46	GENIC	homozygous	111859873
16	73572641	73572642	T	C	41	GENIC	homozygous	111859874
16	73572734	73572735	G	A	53	GENIC	homozygous	111859875
16	73573051	73573052	G	A	59	GENIC	homozygous	112221347
16	73573436	73573437	A	C	50	GENIC	possibly homozygous	111859876
16	73573502	73573503	A	G	53	GENIC	homozygous	111859878
16	73573975	73573980	GGTGA		46	GENIC	homozygous	133781021
16	73573998	73573999	T	G	51	GENIC	homozygous	111859880
16	73575205	73575206	A	G	44	GENIC	homozygous	111859882
16	73575215	73575216	T	C	46	GENIC	homozygous	111859883
16	73576183	73576184	T	C	54	GENIC	homozygous	111859884
16	73576190	73576191	C	T	53	GENIC	homozygous	112221348
16	73577088	73577089	A	G	48	GENIC	homozygous	111859885
16	73577488	73577489	T	A	51	GENIC	homozygous	111859886
16	73577501	73577502	A	T	53	GENIC	homozygous	112221349
16	73578485	73578486	T	C	57	GENIC	homozygous	111859887
16	73578710	73578711	A	T	68	GENIC	homozygous	111859888
16	73578726	73578727	G	T	65	GENIC	homozygous	112221350
16	73578330	73578331	G	A	39	GENIC	homozygous	112030543