chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	20795053	20795054	A	G	19	GENIC	homozygous	110985959
17	20797667	20797668	T	C	14	GENIC	homozygous	111177707
17	20797889	20797890	T	C	14	GENIC	homozygous	110985961
17	20797949	20797950	T	C	14	GENIC	homozygous	110985963
17	20797950	20797951	T	C	14	GENIC	homozygous	110985965
17	20798841	20798842	C	G	14	GENIC	homozygous	110985967
17	20798894	20798895	T	C	16	GENIC	homozygous	110985969
17	20798907	20798908	C	T	13	GENIC	homozygous	110985971
17	20799056	20799057	A	G	16	GENIC	homozygous	110985973
17	20807198	20807199	C	G	13	GENIC	homozygous	111234100
17	20807454	20807455	A	C	18	GENIC	possibly homozygous	110985975
17	20807576	20807577	G	A	14	GENIC	homozygous	110985977
17	20807669	20807670	T	G	25	GENIC	homozygous	110985979
17	20807749	20807750	A	T	29	GENIC	homozygous	110985981
17	20808718	20808719	G	A	17	GENIC	homozygous	110985983
17	20809044	20809045	G	A	26	GENIC	homozygous	110985985
17	20809177	20809178	C	T	20	GENIC	homozygous	110985987
17	20809223	20809224	T	C	26	GENIC	homozygous	110985989
17	20810150	20810151	T	C	8	GENIC	homozygous	110985991
17	20811997	20811998	T	C	10	GENIC	homozygous	110985993
17	20812293	20812294	T	C	9	GENIC	homozygous	110985995
17	20812941	20812942	C	T	22	GENIC	homozygous	110985997
17	20813294	20813295	G	A	19	GENIC	homozygous	110985999
17	20806977	20806978	T	G	12	GENIC	homozygous	111398714
17	20807300	20807301	A	C	9	GENIC	homozygous	111338144