chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	75496039	75496040	A	G	10	GENIC	homozygous	116639113
10	75496892	75496893	C	G	20	GENIC	homozygous	116800410
10	75497655	75497656	G	A	17	GENIC	homozygous	116800412
10	75502714	75502715	G	A	19	GENIC	homozygous	116639146
10	75505079	75505080	T	C	17	GENIC	homozygous	116639150
10	75506624	75506625	T	G	26	GENIC	homozygous	116639156
10	75507244	75507245	G	A	29	GENIC	possibly homozygous	116800416
10	75507588	75507589	T	C	26	GENIC	homozygous	116639160
10	75507895	75507896	T	C	24	GENIC	homozygous	116639162
10	75510395	75510396	A	G	31	GENIC	homozygous	116639168
10	75512361	75512362	A	G	26	GENIC	homozygous	116800418
10	75512646	75512647	G	A	25	GENIC	homozygous	116800420
10	75513021	75513022	G	A	25	GENIC	homozygous	116800422
10	75513231	75513232	T	C	26	GENIC	homozygous	116639172
10	75513310	75513311	T	C	10	GENIC	homozygous	116800424
10	75513467	75513468	G	T	13	GENIC	homozygous	116639174
10	75513685	75513686	A	G	15	GENIC	homozygous	116639176
10	75514600	75514601	T	C	22	GENIC	homozygous	116639182
10	75514614	75514615	T	C	19	GENIC	homozygous	116800426
10	75514731	75514732	C	G	9	GENIC	homozygous	117104710
10	75515597	75515598	C	T	29	GENIC	homozygous	116800428
10	75515627	75515628	C	T	33	GENIC	homozygous	116800430
10	75515890	75515891	T	C	28	GENIC	homozygous	116639190