chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108396766	108396767	T	C	9	GENIC	homozygous	51596096
10	108397090	108397091	G	T	9	GENIC	homozygous	51596098
10	108397871	108397872	C	T	9	GENIC	homozygous	51596100
10	108397987	108397988	C	T	6	GENIC	homozygous	51596102
10	108398368	108398369	A	G	5	GENIC	homozygous	51596104
10	108398863	108398864	T	C	19	GENIC	homozygous	51596106
10	108399592	108399593	C	T	10	GENIC	homozygous	51596108
10	108400449	108400450	A	G	9	GENIC	homozygous	51596112
10	108401486	108401487	T	C	11	GENIC	possibly homozygous	51596116
10	108402283	108402284	A	G	8	GENIC	homozygous	51596118
10	108403550	108403551	T	TAAC	2	GENIC	homozygous	51596120
10	108403553	108403554	G	GGGCTAC	1	GENIC	homozygous	51596122
10	108403922	108403924	AA	--	9	GENIC	homozygous	51596124
10	108405663	108405664	T	TC	7	GENIC	homozygous	51596126
10	108407879	108407880	A	T	12	GENIC	heterozygous	51596132
10	108409485	108409486	A	G	16	GENIC	possibly homozygous	51596140
10	108410258	108410259	T	A	14	GENIC	heterozygous	51596142
10	108411238	108411239	G	A	14	GENIC	homozygous	51596144
10	108412065	108412066	G	A	3	GENIC	heterozygous	51596148
10	108412067	108412068	C	CT	2	GENIC	homozygous	51596149
10	108412524	108412525	C	T	19	GENIC	homozygous	51596151
10	108412774	108412775	T	C	7	GENIC	homozygous	51596153