chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	9517436	9517437	A	C	29	GENIC	homozygous	48499027
14	9518488	9518489	C	T	30	GENIC	possibly homozygous	48499029
14	9518537	9518538	A	T	33	GENIC	homozygous	48499031
14	9518644	9518645	C	T	41	GENIC	homozygous	48499033
14	9518645	9518646	A	T	41	GENIC	homozygous	48499035
14	9519300	9519301	A	G	49	GENIC	homozygous	48499037
14	9519429	9519430	C	A	50	GENIC	homozygous	48499039
14	9519574	9519575	A	G	34	GENIC	homozygous	48499041
14	9519590	9519591	A	C	34	GENIC	homozygous	48499043
14	9520198	9520199	T	G	54	GENIC	homozygous	48499045
14	9520298	9520299	A	G	47	GENIC	homozygous	48499047
14	9521028	9521029	C	T	34	GENIC	possibly homozygous	48499054
14	9520573	9520574	A	G	22	GENIC	homozygous	48499049
14	9520612	9520613	T	TA	16	GENIC	homozygous	48499050
14	9520987	9520988	C	CTGTG	12	GENIC	possibly homozygous	48499052
14	9521030	9521031	C	T	29	GENIC	homozygous	48499056
14	9521095	9521096	T	C	28	GENIC	homozygous	48499058
14	9521193	9521194	T	-	34	GENIC	homozygous	48499060
14	9521240	9521241	T	G	30	GENIC	homozygous	48499062
14	9521529	9521533	GGGA	----	23	GENIC	homozygous	48499064
14	9521530	9521533	GGA	---	23	GENIC	homozygous	48499066
14	9521538	9521539	T	C	26	GENIC	homozygous	48499068
14	9521818	9521819	G	A	39	GENIC	homozygous	48499070
14	9522357	9522358	G	C	51	GENIC	homozygous	48499072
14	9522602	9522603	T	TC	16	GENIC	homozygous	48499074
14	9523271	9523272	G	T	41	GENIC	homozygous	48499076
14	9523430	9523431	T	C	28	GENIC	homozygous	48499078
14	9523438	9523439	G	A	26	GENIC	homozygous	48499080
14	9523578	9523579	T	-	30	GENIC	homozygous	48499082