chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	65898641	65898642	G	GCGACTCGCGACT	10	GENIC	homozygous	55437208
5	65898654	65898655	T	A	18	GENIC	homozygous	55437210
5	65899782	65899783	C	T	63	GENIC	homozygous	55437212
5	65900110	65900111	C	T	42	GENIC	homozygous	55437214
5	65900111	65900112	A	G	43	GENIC	homozygous	55437216
5	65900134	65900135	T	TG	48	GENIC	homozygous	55437218
5	65900178	65900179	C	T	44	GENIC	homozygous	55437220
5	65900644	65900645	C	CG	34	GENIC	homozygous	55437222
5	65900822	65900823	T	G	58	GENIC	homozygous	55437224
5	65900839	65900840	G	A	60	GENIC	homozygous	55437226
5	65901263	65901264	T	C	62	GENIC	homozygous	55437228
5	65901644	65901645	G	A	46	GENIC	homozygous	55437230
5	65901839	65901840	A	G	31	GENIC	homozygous	55437232
5	65902118	65902119	G	A	44	GENIC	homozygous	55437234
5	65902181	65902182	A	G	52	GENIC	homozygous	55437236
5	65902208	65902209	T	C	45	GENIC	homozygous	55437238
5	65902436	65902437	T	C	42	GENIC	homozygous	55437240
5	65902713	65902714	A	G	40	GENIC	possibly homozygous	55437242
5	65902715	65902716	T	C	37	GENIC	homozygous	55437244
5	65902976	65902977	A	G	51	GENIC	homozygous	55437246
5	65903116	65903117	G	A	34	GENIC	homozygous	55437248
5	65903313	65903314	T	C	49	GENIC	homozygous	55437250
5	65903423	65903424	T	C	49	GENIC	homozygous	55437252