chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	12261265	12261265		A	29	GENIC	possibly homozygous	129423635
17	12261740	12261741	G		19	GENIC	homozygous	129423636
17	12262541	12262541		C	8	GENIC	homozygous	129423637
17	12262567	12262568	T		9	GENIC	homozygous	129423638
17	12262639	12262639		A	16	GENIC	homozygous	129423639
17	12262642	12262642		CT	16	GENIC	homozygous	129423640
17	12262649	12262649		C	17	GENIC	homozygous	129423641
17	12262686	12262686		T	17	GENIC	possibly homozygous	129423642
17	12263120	12263121	C		27	GENIC	homozygous	129423644
17	12263141	12263141		C	24	GENIC	homozygous	129423645
17	12263146	12263146		G	25	GENIC	homozygous	129423646
17	12263153	12263154	C		26	GENIC	homozygous	129423647
17	12263157	12263157		C	26	GENIC	homozygous	129423648
17	12263164	12263164		G	25	GENIC	homozygous	129423649
17	12263179	12263179		G	25	GENIC	homozygous	129423650
17	12263190	12263190		G	25	GENIC	homozygous	129423651
17	12263210	12263211	A		30	GENIC	homozygous	129423652
17	12263215	12263215		A	31	GENIC	homozygous	129423653
17	12263244	12263244		G	28	GENIC	homozygous	129423654
17	12263256	12263257	C		31	GENIC	homozygous	129423655
17	12263261	12263269	AAGGTATC		31	GENIC	homozygous	129423656
17	12263279	12263281	CT		34	GENIC	homozygous	129423657
17	12262597	12262598	A	C	18	GENIC	homozygous	111295162
17	12263242	12263243	C	G	29	GENIC	homozygous	111295163
17	12263253	12263254	A	C	30	GENIC	homozygous	111295164
17	12262598	12262599	C	A	18	GENIC	homozygous	111315144
17	12263125	12263126	G	C	27	GENIC	homozygous	119264966
17	12266016	12266017	C	T	45	GENIC	homozygous	110959539
17	12266046	12266047	C	T	41	GENIC	homozygous	110959541
17	12266875	12266876	C	A	40	GENIC	homozygous	110959543
17	12266876	12266877	G	C	42	GENIC	homozygous	110959545
17	12267265	12267266	T	C	50	GENIC	homozygous	110959547
17	12270188	12270189	A	G	30	GENIC	homozygous	110959549
17	12273871	12273872	G	A	41	GENIC	homozygous	110959551