chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	12261265	12261265		A	11	GENIC	possibly homozygous	129423635
17	12261740	12261741	G		12	GENIC	homozygous	129423636
17	12262541	12262541		C	2	GENIC	homozygous	129423637
17	12262567	12262568	T		2	GENIC	homozygous	129423638
17	12262597	12262598	A	C	6	GENIC	homozygous	111295162
17	12262598	12262599	C	A	6	GENIC	homozygous	111315144
17	12262639	12262639		A	6	GENIC	homozygous	129423639
17	12262642	12262642		CT	6	GENIC	homozygous	129423640
17	12262649	12262649		C	6	GENIC	homozygous	129423641
17	12262686	12262686		T	7	GENIC	homozygous	129423642
17	12262714	12262714		C	11	GENIC	homozygous	129423643
17	12262733	12262734	G	A	10	GENIC	homozygous	130168617
17	12263242	12263243	C	G	21	GENIC	homozygous	111295163
17	12263244	12263244		G	21	GENIC	homozygous	129423654
17	12263253	12263254	A	C	20	GENIC	homozygous	111295164
17	12263256	12263257	C		21	GENIC	homozygous	129423655
17	12263261	12263269	AAGGTATC		19	GENIC	homozygous	129423656
17	12263279	12263281	CT		19	GENIC	homozygous	129423657
17	12266876	12266877	G	C	33	GENIC	homozygous	110959545
17	12262732	12262732		C	10	GENIC	homozygous	130165015
17	12262754	12262755	G		7	GENIC	homozygous	130165016
17	12266016	12266017	C	T	26	GENIC	homozygous	110959539
17	12266046	12266047	C	T	21	GENIC	homozygous	110959541
17	12266875	12266876	C	A	31	GENIC	homozygous	110959543
17	12267265	12267266	T	C	17	GENIC	homozygous	110959547
17	12270188	12270189	A	G	16	GENIC	homozygous	110959549
17	12273871	12273872	G	A	19	GENIC	homozygous	110959551