chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	47942792	47942793	C	T	21	GENIC	homozygous	54379520
7	47943004	47943005	C	T	29	GENIC	homozygous	54379522
7	47943213	47943218	TTTAG	-----	25	GENIC	homozygous	54379524
7	47943354	47943356	AA	--	24	GENIC	possibly homozygous	54379526
7	47943355	47943356	A	-	24	GENIC	heterozygous	54898034
7	47943578	47943579	T	A	28	GENIC	homozygous	54379528
7	47945437	47945438	G	A	28	GENIC	homozygous	54379530
7	47946053	47946054	G	A	42	GENIC	homozygous	54379532
7	47946074	47946075	T	TTA	40	GENIC	homozygous	54379534
7	47946194	47946195	A	G	25	GENIC	homozygous	54379536
7	47946257	47946258	C	G	21	GENIC	homozygous	54379538
7	47946803	47946804	A	-	34	GENIC	possibly homozygous	54379540
7	47946873	47946874	A	G	35	GENIC	homozygous	53911316
7	47947003	47947004	C	T	24	GENIC	homozygous	54379542
7	47947071	47947072	C	T	29	GENIC	homozygous	54379544
7	47947120	47947121	A	G	34	GENIC	homozygous	53911317
7	47947138	47947139	G	A	29	GENIC	homozygous	54379546
7	47947328	47947329	G	T	29	GENIC	homozygous	53911318
7	47947706	47947707	T	TTGTC	34	GENIC	homozygous	53911320
7	47948077	47948078	T	C	30	GENIC	homozygous	54379548
7	47948296	47948297	T	C	20	GENIC	homozygous	54379550
7	47948960	47948961	T	C	17	GENIC	homozygous	54379552