chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39565384	39565385	T	C	56	GENIC	homozygous	138771180
10	39565608	39565609	C	T	40	GENIC	homozygous	138771181
10	39566122	39566123	G	C	51	GENIC	homozygous	138771182
10	39567095	39567096	G	A	31	GENIC	homozygous	138771183
10	39568198	39568199	A	G	45	GENIC	homozygous	138771184
10	39571177	39571178	A	C	44	GENIC	homozygous	138771185
10	39573059	39573060	A	C	39	GENIC	homozygous	138771186
10	39574800	39574801	C	T	45	GENIC	homozygous	138771187
10	39575176	39575177	C	T	42	GENIC	homozygous	138771188
10	39575650	39575651	A	T	36	GENIC	homozygous	138771189
10	39576096	39576097	T	C	51	GENIC	homozygous	138771190
10	39576475	39576476	C	T	46	GENIC	homozygous	138771191
10	39577231	39577232	A	G	41	GENIC	homozygous	138771192
10	39577619	39577620	C	T	38	GENIC	homozygous	138771193
10	39576903	39576904	A	G	26	GENIC	heterozygous	403633570
10	39574872	39574873	C	T	38	GENIC	homozygous	146952312
10	39576903	39576904	A		26	GENIC	heterozygous	403633569
10	39569673	39569678	TCTGT		21	GENIC	homozygous	138679864
10	39569416	39569424	GTGTGTGC		22	GENIC	homozygous	146934428
10	39572662	39572663	C		35	GENIC	homozygous	146934429