chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88778153	88778154	T	A	35	GENIC	homozygous	51730718
10	88778257	88778258	T	G	39	GENIC	homozygous	51536061
10	88778931	88778932	T	C	29	GENIC	homozygous	51730720
10	88779246	88779247	G	T	39	GENIC	homozygous	51730722
10	88779371	88779372	T	TC	19	GENIC	heterozygous	51536062
10	88779428	88779429	G	T	16	GENIC	homozygous	51730726
10	88779450	88779451	T	C	15	GENIC	homozygous	51730728
10	88779637	88779638	T	C	22	GENIC	homozygous	51730730
10	88779671	88779672	G	A	27	GENIC	homozygous	51730732
10	88780095	88780096	A	G	29	GENIC	homozygous	51730734
10	88780124	88780125	C	T	29	GENIC	homozygous	51730736
10	88780183	88780185	CC	--	13	GENIC	homozygous	51536066
10	88780339	88780340	A	G	20	GENIC	homozygous	51536067
10	88781652	88781653	T	C	15	GENIC	homozygous	51730738
10	88781688	88781689	A	ACCTC	7	GENIC	possibly homozygous	51730740
10	88782206	88782207	T	TAAAA	11	GENIC	heterozygous	51730742
10	88782710	88782711	C	CTTGT	8	GENIC	homozygous	51730746
10	88784187	88784188	G	T	26	GENIC	homozygous	51730748
10	88785241	88785242	G	GAGA	29	GENIC	homozygous	51536070
10	88785339	88785340	C	T	36	GENIC	homozygous	51730750
10	88782206	88782207	T	TAAA	11	GENIC	heterozygous	52394142
10	88781688	88781689	A	ACCTCC	7	GENIC	heterozygous	52507902