chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	137148586	137148587	C	T	16	GENIC	homozygous	54837917
7	137148798	137148799	A	G	11	GENIC	homozygous	54253975
7	137148956	137148957	T	A	14	GENIC	possibly homozygous	54137602
7	137149002	137149003	T	G	4	GENIC	homozygous	54137604
7	137149347	137149349	AA	--	6	GENIC	heterozygous	54837919
7	137149410	137149411	A	T	2	GENIC	homozygous	54253989
7	137149534	137149535	G	A	14	GENIC	heterozygous	54837921
7	137149644	137149645	G	A	7	GENIC	possibly homozygous	54837923
7	137149935	137149936	A	T	17	GENIC	homozygous	54137608
7	137149997	137149998	C	CTTGTTTGT	1	GENIC	homozygous	54137612
7	137150134	137150135	T	-	1	GENIC	homozygous	54137613
7	137150222	137150223	T	G	3	GENIC	heterozygous	54837925
7	137150351	137150352	A	G	10	GENIC	homozygous	54254003
7	137151268	137151269	G	A	22	GENIC	homozygous	54837927
7	137151311	137151312	G	GTGTC	8	GENIC	homozygous	54254015
7	137151529	137151530	G	A	28	GENIC	homozygous	54837929
7	137151732	137151733	G	A	18	GENIC	possibly homozygous	54837931
7	137152728	137152729	A	G	9	GENIC	possibly homozygous	54137627
7	137152946	137152947	A	G	21	GENIC	possibly homozygous	54137630
7	137153127	137153128	G	A	22	GENIC	homozygous	54837939
7	137153207	137153208	G	GA	3	GENIC	heterozygous	54254054
7	137153658	137153659	C	A	33	GENIC	homozygous	54837941
7	137153697	137153698	T	A	27	GENIC	possibly homozygous	54137633
7	137153848	137153849	G	A	18	GENIC	homozygous	54837943
7	137154398	137154399	C	T	21	GENIC	possibly homozygous	54137637
7	137154438	137154439	T	G	24	GENIC	homozygous	54137638