chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	9517031	9517032	C	G	7	GENIC	homozygous	49272622
14	9517436	9517437	A	C	13	GENIC	homozygous	48499027
14	9518488	9518489	C	T	7	GENIC	homozygous	48499029
14	9520198	9520199	T	G	15	GENIC	homozygous	48499045
14	9520298	9520299	A	G	18	GENIC	homozygous	48499047
14	9520986	9520987	C	T	14	GENIC	homozygous	49571293
14	9520573	9520574	A	G	27	GENIC	homozygous	48499049
14	9520612	9520613	T	TA	18	GENIC	possibly homozygous	48499050
14	9520987	9520988	C	CTGTG	3	GENIC	heterozygous	48499052
14	9520987	9520988	C	CTG	3	GENIC	heterozygous	49423947
14	9521028	9521029	C	T	4	GENIC	homozygous	48499054
14	9521030	9521031	C	T	4	GENIC	homozygous	48499056
14	9521095	9521096	T	C	22	GENIC	homozygous	48499058
14	9521193	9521194	T	-	17	GENIC	homozygous	48499060
14	9521240	9521241	T	G	30	GENIC	homozygous	48499062
14	9521522	9521523	G	-	11	GENIC	homozygous	49272631
14	9521549	9521550	A	G	19	GENIC	homozygous	49571294
14	9522602	9522603	T	TC	7	GENIC	homozygous	48499074
14	9522687	9522692	GGGGA	-----	10	GENIC	homozygous	49571295
14	9523271	9523272	G	T	19	GENIC	homozygous	48499076
14	9523430	9523431	T	C	16	GENIC	homozygous	48499078
14	9523578	9523579	T	-	26	GENIC	homozygous	48499082