chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88778153	88778154	T	A	10	GENIC	possibly homozygous	51730718
10	88778257	88778258	T	G	14	GENIC	homozygous	51536061
10	88778931	88778932	T	C	46	GENIC	homozygous	51730720
10	88779246	88779247	G	T	43	GENIC	homozygous	51730722
10	88779371	88779372	T	TC	16	GENIC	possibly homozygous	51536062
10	88779392	88779396	TTTT	----	11	GENIC	possibly homozygous	51730724
10	88779428	88779429	G	T	20	GENIC	homozygous	51730726
10	88779450	88779451	T	C	22	GENIC	homozygous	51730728
10	88779637	88779638	T	C	47	GENIC	possibly homozygous	51730730
10	88779671	88779672	G	A	51	GENIC	possibly homozygous	51730732
10	88780095	88780096	A	G	34	GENIC	homozygous	51730734
10	88780124	88780125	C	T	36	GENIC	possibly homozygous	51730736
10	88780183	88780185	CC	--	22	GENIC	homozygous	51536066
10	88780339	88780340	A	G	48	GENIC	homozygous	51536067
10	88781652	88781653	T	C	40	GENIC	homozygous	51730738
10	88781688	88781689	A	ACCTC	13	GENIC	homozygous	51730740
10	88782206	88782207	T	TAAAA	8	GENIC	possibly homozygous	51730742
10	88782206	88782207	T	TAA	8	GENIC	heterozygous	51924985
10	88782710	88782711	C	CTTGT	28	GENIC	homozygous	51730746
10	88784187	88784188	G	T	40	GENIC	homozygous	51730748
10	88785241	88785242	G	GAGA	44	GENIC	homozygous	51536070
10	88785339	88785340	C	T	45	GENIC	homozygous	51730750