chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	125048666	125048667	T	C	25	GENIC	homozygous	54095975
7	125048786	125048787	G	A	29	GENIC	possibly homozygous	54751193
7	125048936	125048937	G	T	11	GENIC	heterozygous	54095976
7	125050478	125050479	G	T	21	GENIC	possibly homozygous	54095985
7	125052214	125052215	T	TGGAG	1	GENIC	homozygous	54095989
7	125054097	125054098	G	C	12	GENIC	homozygous	54751201
7	125055836	125055837	G	C	6	GENIC	heterozygous	54751203
7	125055845	125055846	A	G	5	GENIC	homozygous	54095994
7	125055846	125055847	T	TG	5	GENIC	heterozygous	54751205
7	125055851	125055852	A	G	8	GENIC	homozygous	54095995
7	125057462	125057463	A	G	8	GENIC	homozygous	54095997
7	125057782	125057783	C	T	11	GENIC	homozygous	54751207
7	125058073	125058097	TGGGGCAGGCTGTGGGGCAGGCTG	------------------------	1	GENIC	homozygous	55004882
7	125058254	125058255	C	T	11	GENIC	homozygous	54751209
7	125058519	125058520	T	C	8	GENIC	possibly homozygous	54095998
7	125059731	125059732	G	GC	10	GENIC	homozygous	54096000
7	125062164	125062165	G	A	6	GENIC	heterozygous	54751211
7	125063395	125063396	G	A	13	GENIC	homozygous	54751213
7	125063609	125063610	G	A	9	GENIC	possibly homozygous	54751215
7	125065231	125065232	T	C	14	GENIC	homozygous	54096018
7	125066925	125066926	G	C	6	GENIC	homozygous	54096020
7	125066951	125066952	T	A	13	GENIC	possibly homozygous	54751217
7	125068721	125068722	T	C	21	GENIC	possibly homozygous	54096027
7	125070527	125070528	T	G	13	GENIC	heterozygous	54096029