chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13724121	13724122	A	G	9	INTERGENIC	homozygous	51621980
10	13725217	13725218	A	ACAAT	10	INTERGENIC	homozygous	51621982
10	13727496	13727497	A	AATTTT	15	INTERGENIC	homozygous	52431459
10	13729944	13729945	T	TAAAG	9	INTERGENIC	homozygous	51621990
10	13729952	13729953	T	G	12	INTERGENIC	homozygous	51621991
10	13731051	13731052	C	T	14	GENIC	homozygous	51621994
10	13731131	13731132	T	-	10	GENIC	homozygous	51621995
10	13731439	13731440	T	C	8	GENIC	homozygous	51621996
10	13731501	13731502	T	G	11	GENIC	homozygous	51621997
10	13734386	13734387	G	A	21	GENIC	homozygous	51621999
10	13736905	13736906	G	-	7	GENIC	homozygous	51622007
10	13736915	13736916	C	T	7	GENIC	homozygous	51622008
10	13737079	13737080	A	AG	16	GENIC	homozygous	51622009
10	13737116	13737117	C	A	14	GENIC	homozygous	51622010
10	13737358	13737359	T	TA	7	GENIC	homozygous	51622011
10	13738801	13738802	T	C	16	GENIC	homozygous	51622013
10	13739417	13739418	G	-	13	GENIC	homozygous	51622014
10	13740889	13740890	T	C	14	GENIC	homozygous	51622015
10	13743184	13743185	A	T	12	GENIC	homozygous	51622016
10	13743341	13743342	C	T	13	GENIC	homozygous	51622017
10	13744646	13744647	A	G	8	GENIC	homozygous	51329051
10	13747994	13747995	T	C	10	GENIC	homozygous	51622022
10	13751768	13751769	A	G	12	GENIC	homozygous	51622023
10	13752374	13752375	A	G	17	GENIC	homozygous	51622026
10	13752557	13752558	G	A	20	GENIC	homozygous	51622027
10	13755854	13755855	T	C	12	GENIC	homozygous	51622028
10	13758145	13758146	A	G	13	GENIC	homozygous	51622029
10	13764875	13764876	A	G	14	GENIC	homozygous	51809499
10	13764985	13764986	T	C	12	GENIC	homozygous	51622030
10	13764992	13764993	A	C	12	GENIC	homozygous	51622031
10	13768411	13768412	A	G	15	GENIC	homozygous	51622033
10	13774854	13774855	G	C	19	GENIC	homozygous	51622035
10	13779536	13779537	T	C	10	GENIC	homozygous	51622036
10	13739421	13739422	G	A	13	GENIC	homozygous	53540529