chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	21704245	21704249	CTCT	----	1	GENIC	homozygous	47728422
17	21705930	21705931	T	G	16	GENIC	homozygous	47050747
17	21707687	21707688	G	A	19	GENIC	heterozygous	47050749
17	21710431	21710432	T	G	17	GENIC	possibly homozygous	47050751
17	21713491	21713492	T	C	20	GENIC	possibly homozygous	47050753
17	21714083	21714084	C	T	10	GENIC	homozygous	47050754
17	21714542	21714543	A	-	9	GENIC	homozygous	47050755
17	21714597	21714598	G	-	4	GENIC	heterozygous	47050757
17	21714624	21714625	A	C	4	GENIC	homozygous	47050758
17	21714636	21714637	A	-	1	GENIC	homozygous	47050759
17	21714643	21714644	A	-	2	GENIC	homozygous	47050760
17	21714690	21714691	A	AT	10	GENIC	possibly homozygous	47050761
17	21718011	21718012	A	-	7	GENIC	heterozygous	47380508
17	21719334	21719337	AGC	---	3	GENIC	heterozygous	47050768
17	21721294	21721295	A	G	11	GENIC	homozygous	47050770
17	21721754	21721755	T	C	17	GENIC	heterozygous	47050773
17	21721989	21721990	A	G	18	GENIC	possibly homozygous	47050774
17	21722780	21722781	C	CT	1	GENIC	homozygous	47050778
17	21722962	21722963	G	A	2	GENIC	homozygous	47050782
17	21723929	21723930	T	A	21	GENIC	homozygous	47050783
17	21724255	21724256	T	C	22	GENIC	homozygous	47050784
17	21724711	21724712	G	GT	1	GENIC	homozygous	47050785