chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	49932011	49932012	C	T	26	GENIC	homozygous	46260501
19	49937191	49937192	T	A	22	GENIC	homozygous	46260502
19	49937344	49937348	AACT	----	2	GENIC	homozygous	46153049
19	49937563	49937564	A	C	17	GENIC	homozygous	46260503
19	49937700	49937711	TTTTTTTTTGT	-----------	4	GENIC	heterozygous	46260504
19	49937769	49937770	C	A	16	GENIC	possibly homozygous	46260506
19	49937993	49937994	T	C	19	GENIC	homozygous	46260507
19	49938173	49938174	A	C	19	GENIC	homozygous	46260508
19	49938213	49938214	C	T	4	GENIC	homozygous	46260509
19	49938216	49938217	T	C	4	GENIC	heterozygous	46260510
19	49938296	49938297	A	G	11	GENIC	heterozygous	46260511
19	49938400	49938401	A	G	13	GENIC	homozygous	46260512
19	49938481	49938482	T	G	17	GENIC	possibly homozygous	46260513
19	49938628	49938629	A	G	21	GENIC	possibly homozygous	46260514
19	49938702	49938703	A	C	10	GENIC	possibly homozygous	46260515
19	49938740	49938741	A	G	20	GENIC	homozygous	46260516
19	49938767	49938768	C	T	12	GENIC	possibly homozygous	46260517
19	49938787	49938790	CTC	---	8	GENIC	heterozygous	46260518
19	49941757	49941758	G	A	9	GENIC	homozygous	46260520
19	49941437	49941438	C	-	11	GENIC	possibly homozygous	46260519