chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	73564408	73564409	A	G	20	GENIC	homozygous	111859858
16	73565625	73565626	T	C	21	GENIC	homozygous	111859859
16	73565705	73565706	A	G	25	GENIC	homozygous	111859860
16	73566227	73566228	C	T	20	GENIC	homozygous	112234754
16	73566530	73566531	C	T	25	GENIC	homozygous	111859861
16	73568021	73568022	T	G	18	GENIC	homozygous	111859864
16	73568444	73568445	G	A	31	GENIC	homozygous	111859865
16	73568646	73568647	G	A	29	GENIC	homozygous	112234756
16	73568838	73568839	A	G	28	GENIC	homozygous	112234758
16	73570337	73570338	G	A	27	GENIC	homozygous	111859867
16	73570982	73570983	G	A	20	GENIC	homozygous	112234762
16	73571059	73571060	G	A	24	GENIC	homozygous	111859868
16	73571135	73571136	C	T	32	GENIC	homozygous	112234764
16	73571530	73571531	A	G	23	GENIC	homozygous	111859869
16	73571531	73571532	A	G	23	GENIC	homozygous	111859870
16	73572189	73572190	T	G	35	GENIC	homozygous	111859872
16	73572305	73572319	TGTTATTTCTCCAT		28	GENIC	homozygous	131181652
16	73572499	73572500	C	T	32	GENIC	homozygous	111859873
16	73572641	73572642	T	C	22	GENIC	possibly homozygous	111859874
16	73572734	73572735	G	A	20	GENIC	possibly homozygous	111859875
16	73573436	73573437	A	C	31	GENIC	homozygous	111859876
16	73573502	73573503	A	G	31	GENIC	homozygous	111859878
16	73573560	73573561	C	T	26	GENIC	homozygous	112234766
16	73573998	73573999	T	G	28	GENIC	homozygous	111859880
16	73575205	73575206	A	G	29	GENIC	homozygous	111859882
16	73575215	73575216	T	C	26	GENIC	homozygous	111859883
16	73576183	73576184	T	C	27	GENIC	homozygous	111859884
16	73577088	73577089	A	G	29	GENIC	homozygous	111859885
16	73577488	73577489	T	A	27	GENIC	homozygous	111859886
16	73578485	73578486	T	C	24	GENIC	homozygous	111859887
16	73578661	73578662	T	C	28	GENIC	homozygous	112234768
16	73578710	73578711	A	T	32	GENIC	homozygous	111859888
16	73578330	73578331	G	A	27	GENIC	homozygous	112030543