chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11099759	11099760	T	A	4	GENIC	heterozygous	47018877
17	11099775	11099776	T	TA	5	GENIC	homozygous	47018878
17	11099920	11099921	G	T	3	GENIC	homozygous	47018879
17	11100323	11100327	CACT	----	2	GENIC	heterozygous	47018882
17	11100571	11100572	A	G	8	GENIC	homozygous	47018883
17	11100580	11100581	T	C	10	GENIC	homozygous	47018884
17	11101143	11101144	C	G	15	GENIC	homozygous	47018885
17	11101552	11101553	C	T	10	GENIC	heterozygous	47018886
17	11101695	11101698	CCA	---	6	GENIC	heterozygous	47018887
17	11101850	11101851	C	A	11	GENIC	possibly homozygous	47018888
17	11101996	11101997	A	AAC	1	GENIC	homozygous	47018889
17	11102082	11102083	T	C	13	GENIC	heterozygous	47018891
17	11102187	11102188	T	C	5	GENIC	homozygous	47018892
17	11102266	11102267	A	G	12	GENIC	homozygous	47018893
17	11102417	11102418	G	-	5	GENIC	homozygous	47018895
17	11102513	11102514	C	A	6	GENIC	heterozygous	47018896
17	11102562	11102563	C	T	5	GENIC	homozygous	47018897
17	11104066	11104068	CA	--	3	GENIC	homozygous	47018898