chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106212900	106212901	A	G	55	GENIC	homozygous	144876158
10	106212951	106212952	C	T	47	GENIC	homozygous	144876159
10	106214866	106214867	G	T	62	GENIC	possibly homozygous	144876160
10	106214981	106214982	G	C	59	GENIC	homozygous	144876161
10	106215950	106215951	C	T	52	GENIC	homozygous	144876162
10	106216171	106216172	C	A	75	GENIC	possibly homozygous	144876163
10	106216591	106216592	T	C	53	GENIC	homozygous	144876164
10	106216626	106216626		GAG	48	GENIC	homozygous	144858360
10	106216875	106216876	T	C	55	GENIC	homozygous	144876165
10	106216965	106216966	C	T	39	GENIC	homozygous	144876166
10	106217259	106217260	A	T	32	GENIC	homozygous	144876167
10	106217761	106217762	G	A	51	GENIC	homozygous	144876168
10	106218586	106218586		ACC	51	GENIC	homozygous	144858361
10	106218588	106218588		AACCCTAACCCTAACCC	52	GENIC	homozygous	144858362
10	106218590	106218591	G		47	GENIC	homozygous	144858363
10	106219618	106219618		C	45	GENIC	homozygous	144858364
10	106220118	106220119	T	C	66	GENIC	homozygous	144876169
10	106220676	106220677	G	A	59	GENIC	homozygous	138868441
10	106220788	106220789	G	A	67	GENIC	homozygous	144876170
10	106221112	106221113	T	C	65	GENIC	homozygous	144876171