chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	67154743	67154749	TGTGTT	------	15	GENIC	heterozygous	52383113
10	67154923	67154924	G	GTCGCTCCAGCCC	29	GENIC	homozygous	51480516
10	67154929	67154930	G	C	30	GENIC	homozygous	51680489
10	67155128	67155129	G	C	38	GENIC	homozygous	51480517
10	67155518	67155519	G	A	24	GENIC	homozygous	51680491
10	67156124	67156125	C	CATTGATTG	20	GENIC	homozygous	52383115
10	67156153	67156154	A	ATATC	7	GENIC	homozygous	52383117
10	67156687	67156688	T	C	28	GENIC	homozygous	51680493
10	67156745	67156746	T	C	28	GENIC	homozygous	51680495
10	67157555	67157556	T	C	19	GENIC	heterozygous	52196977
10	67157711	67157712	C	CCGGTGGGCGAAGGCA	22	GENIC	homozygous	51680499
10	67158005	67158006	T	-	11	GENIC	possibly homozygous	51909340
10	67158541	67158542	G	GA	8	GENIC	homozygous	51909342
10	67158564	67158565	C	A	11	GENIC	homozygous	51680503
10	67159174	67159175	A	-	35	GENIC	homozygous	51909343
10	67159611	67159619	TGTATGTA	--------	45	GENIC	homozygous	52320448
10	67159631	67159632	T	C	45	GENIC	homozygous	51909349
10	67159864	67159865	G	A	33	GENIC	homozygous	51909351
10	67160652	67160653	A	G	1	GENIC	homozygous	51909355
10	67160658	67160659	G	-	1	GENIC	homozygous	51909357
10	67160785	67160786	A	G	11	GENIC	possibly homozygous	51909365
10	67161086	67161087	T	-	34	GENIC	homozygous	51909367
10	67161223	67161224	T	G	30	GENIC	homozygous	51680516
10	67161954	67161957	TTG	---	19	GENIC	heterozygous	51680525
10	67162089	67162090	G	A	18	GENIC	homozygous	51909369
10	67162304	67162312	AAACAAAC	--------	23	GENIC	homozygous	52320450
10	67162379	67162380	T	C	31	GENIC	homozygous	51680533
10	67162460	67162463	TCC	---	19	GENIC	homozygous	51909371
10	67162865	67162866	G	C	17	GENIC	homozygous	51909373
10	67163146	67163147	A	-	34	GENIC	homozygous	51680535
10	67163457	67163458	G	GCTCGGT	17	GENIC	homozygous	51909375
10	67165397	67165398	G	T	18	GENIC	homozygous	51909381
10	67165558	67165559	T	TG	12	GENIC	homozygous	51680549
10	67165643	67165644	C	T	16	GENIC	homozygous	51909383