chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	205635044	205635045	A	G	11	GENIC	possibly homozygous	62694951
1	205635050	205635051	C	CAA	9	GENIC	heterozygous	61963946
1	205635052	205635053	A	-	9	GENIC	heterozygous	61065165
1	205637156	205637157	T	C	8	GENIC	homozygous	61065166
1	205637350	205637351	A	G	18	GENIC	homozygous	61065167
1	205638359	205638360	A	T	34	GENIC	homozygous	61065169
1	205638415	205638416	T	C	33	GENIC	homozygous	61065170
1	205638542	205638543	A	ATG	27	GENIC	homozygous	61065173
1	205638546	205638547	T	G	28	GENIC	homozygous	61065174
1	205638548	205638549	A	T	28	GENIC	homozygous	61065175
1	205638873	205638874	A	T	29	GENIC	homozygous	61065176
1	205638875	205638876	T	C	28	GENIC	homozygous	61065177
1	205639522	205639523	G	GC	26	GENIC	homozygous	62694952
1	205639593	205639594	A	G	26	GENIC	homozygous	61065178
1	205639988	205639989	A	G	22	GENIC	homozygous	61065179
1	205640374	205640375	T	C	28	GENIC	homozygous	62585438
1	205640832	205640833	A	G	32	GENIC	homozygous	62585439
1	205641557	205641559	AA	--	20	GENIC	possibly homozygous	62585440
1	205642788	205642790	CA	--	31	GENIC	homozygous	62694953
1	205642790	205642791	A	T	31	GENIC	homozygous	62694954
1	205642869	205642870	G	A	31	GENIC	homozygous	62585442
1	205642966	205642967	A	G	25	GENIC	homozygous	61065184
1	205643294	205643295	G	A	25	GENIC	homozygous	62694955
1	205643333	205643334	A	AAAG	29	GENIC	homozygous	61065186
1	205643942	205643943	G	A	30	GENIC	homozygous	61065187
1	205644216	205644217	T	A	44	GENIC	homozygous	62694956
1	205644389	205644390	C	G	20	GENIC	homozygous	62694957