chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	92390238	92390239	C	T	9	GENIC	homozygous	51543704
10	92390671	92390672	A	T	11	GENIC	homozygous	51543705
10	92391120	92391121	G	A	14	GENIC	homozygous	51543706
10	92392316	92392317	G	A	18	GENIC	homozygous	51543708
10	92392799	92392800	T	C	17	GENIC	homozygous	51543710
10	92392983	92392984	T	C	17	GENIC	homozygous	51543711
10	92392992	92392993	T	C	16	GENIC	homozygous	51543712
10	92393191	92393192	G	C	15	GENIC	homozygous	51543713
10	92393219	92393220	T	C	17	GENIC	homozygous	51543714
10	92393483	92393484	A	G	12	GENIC	homozygous	51543717
10	92394473	92394474	G	A	16	GENIC	homozygous	51742072
10	92394696	92394697	T	C	30	GENIC	homozygous	51543720
10	92395847	92395848	C	T	12	GENIC	possibly homozygous	51742074
10	92395850	92395851	A	G	12	GENIC	homozygous	51543723
10	92396260	92396261	C	CT	13	GENIC	homozygous	52323526
10	92397186	92397187	T	C	20	GENIC	homozygous	51543732
10	92397608	92397610	AA	--	13	GENIC	heterozygous	52509325
10	92390649	92390650	A	ATGTATGTATGTATGTATT	6	GENIC	homozygous	52509317
10	92390663	92390664	A	ATGTATGTATG	4	GENIC	homozygous	52509319
10	92397585	92397586	G	GAAA	7	GENIC	possibly homozygous	52509323
10	92392633	92392634	C	G	24	GENIC	homozygous	52208214
10	92394769	92394770	A	G	25	GENIC	homozygous	52208216
10	92397686	92397687	C	T	24	GENIC	homozygous	52208217