chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	125746090	125746091	C	T	38	GENIC	homozygous	54802491
7	125747342	125747343	C	T	25	GENIC	homozygous	54752547
7	125747534	125747535	C	T	25	GENIC	homozygous	54097923
7	125747571	125747572	G	A	31	GENIC	homozygous	54097924
7	125748329	125748330	A	G	24	GENIC	homozygous	54097925
7	125748832	125748833	C	-	2	GENIC	homozygous	54097927
7	125748927	125748928	G	A	35	GENIC	homozygous	54097929
7	125749012	125749013	G	A	18	GENIC	homozygous	54097930
7	125749414	125749415	A	G	19	GENIC	homozygous	54097931
7	125751521	125751522	A	ATT	10	GENIC	heterozygous	54097933
7	125751521	125751522	A	AT	10	GENIC	heterozygous	55005887
7	125752000	125752001	T	C	23	GENIC	homozygous	54097934
7	125752756	125752757	G	A	14	GENIC	homozygous	54097935
7	125753821	125753822	C	T	14	GENIC	homozygous	54097936
7	125753897	125753898	C	T	25	GENIC	homozygous	54097937
7	125753949	125753950	G	A	20	GENIC	homozygous	54097938
7	125754274	125754275	A	G	27	GENIC	homozygous	54097939
7	125754320	125754321	C	T	23	GENIC	homozygous	54097940
7	125754367	125754368	C	T	16	GENIC	homozygous	54097941
7	125754379	125754380	G	C	19	GENIC	homozygous	54097942
7	125755157	125755158	G	A	15	GENIC	possibly homozygous	54097943
7	125755666	125755667	C	T	20	GENIC	homozygous	54097944
7	125755703	125755704	C	T	22	GENIC	homozygous	54097945
7	125756500	125756501	T	C	19	GENIC	homozygous	54097946
7	125756849	125756850	A	G	18	GENIC	homozygous	54097947
7	125756965	125756966	G	GAAAA	10	GENIC	heterozygous	54097949
7	125756965	125756966	G	GA	10	GENIC	heterozygous	55005899
7	125756965	125756966	G	GAAAAAAAAAAA	10	GENIC	heterozygous	55030721
7	125757153	125757154	T	TA	19	GENIC	possibly homozygous	54097950