chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	125048666	125048667	T	C	33	GENIC	homozygous	54095975
7	125048786	125048787	G	A	29	GENIC	homozygous	54751193
7	125048936	125048937	G	T	42	GENIC	homozygous	54095976
7	125049753	125049759	CAAAAA	------	16	GENIC	possibly homozygous	54751195
7	125050478	125050479	G	T	44	GENIC	homozygous	54095985
7	125052214	125052215	T	TGGAG	11	GENIC	possibly homozygous	54095989
7	125052304	125052305	C	T	18	GENIC	homozygous	54751197
7	125054097	125054098	G	C	37	GENIC	homozygous	54751201
7	125055836	125055837	G	C	31	GENIC	homozygous	54751203
7	125055845	125055846	A	G	31	GENIC	homozygous	54095994
7	125055846	125055847	T	TG	30	GENIC	homozygous	54751205
7	125055851	125055852	A	G	31	GENIC	homozygous	54095995
7	125057462	125057463	A	G	41	GENIC	possibly homozygous	54095997
7	125057782	125057783	C	T	28	GENIC	homozygous	54751207
7	125058073	125058097	TGGGGCAGGCTGTGGGGCAGGCTG	------------------------	22	GENIC	homozygous	55004882
7	125058254	125058255	C	T	37	GENIC	possibly homozygous	54751209
7	125058519	125058520	T	C	27	GENIC	homozygous	54095998
7	125059731	125059732	G	GC	33	GENIC	homozygous	54096000
7	125062164	125062165	G	A	41	GENIC	homozygous	54751211
7	125063192	125063200	TGTGTGTG	--------	3	GENIC	homozygous	55097703
7	125063395	125063396	G	A	13	GENIC	homozygous	54751213
7	125063609	125063610	G	A	26	GENIC	possibly homozygous	54751215
7	125065231	125065232	T	C	21	GENIC	homozygous	54096018
7	125066925	125066926	G	C	26	GENIC	homozygous	54096020
7	125066951	125066952	T	A	26	GENIC	homozygous	54751217
7	125068721	125068722	T	C	33	GENIC	homozygous	54096027
7	125070527	125070528	T	G	48	GENIC	homozygous	54096029