chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	9517023	9517024	T	A	17	GENIC	homozygous	49459396
14	9517031	9517032	C	G	17	GENIC	homozygous	49272622
14	9517169	9517170	C	G	24	GENIC	homozygous	49272623
14	9518537	9518538	A	G	29	GENIC	homozygous	49272624
14	9518488	9518489	C	T	15	GENIC	homozygous	48499029
14	9519502	9519503	T	C	29	GENIC	homozygous	49272625
14	9519574	9519575	A	G	30	GENIC	homozygous	48499041
14	9519623	9519624	C	T	34	GENIC	homozygous	49272626
14	9519630	9519631	A	T	33	GENIC	homozygous	49272627
14	9519817	9519818	A	G	29	GENIC	homozygous	49272628
14	9520198	9520199	T	G	17	GENIC	homozygous	48499045
14	9520298	9520299	A	G	24	GENIC	homozygous	48499047
14	9520632	9520633	C	T	28	GENIC	homozygous	49272629
14	9520573	9520574	A	G	23	GENIC	homozygous	48499049
14	9520612	9520613	T	TA	26	GENIC	homozygous	48499050
14	9520987	9520988	C	CTATGTG	9	GENIC	possibly homozygous	49272630
14	9521028	9521029	C	T	3	GENIC	homozygous	48499054
14	9521030	9521031	C	T	3	GENIC	homozygous	48499056
14	9521095	9521096	T	C	26	GENIC	homozygous	48499058
14	9521193	9521194	T	-	6	GENIC	homozygous	48499060
14	9521240	9521241	T	G	14	GENIC	homozygous	48499062
14	9521522	9521523	G	-	19	GENIC	homozygous	49272631
14	9521538	9521539	T	C	17	GENIC	homozygous	48499068
14	9522602	9522603	T	TC	22	GENIC	possibly homozygous	48499074
14	9523271	9523272	G	T	26	GENIC	homozygous	48499076
14	9523430	9523431	T	C	21	GENIC	homozygous	48499078
14	9523578	9523579	T	-	17	GENIC	homozygous	48499082
14	9520987	9520988	C	CTGTGTG	9	GENIC	heterozygous	49298419