chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	23388054	23388057	GGC		42	GENIC	homozygous	131216931
19	23388865	23388866	C	T	35	GENIC	homozygous	109888068
19	23389234	23389235	A	G	26	GENIC	homozygous	109888070
19	23389415	23389415		T	25	GENIC	homozygous	131216932
19	23393319	23393320	G	T	43	GENIC	homozygous	109917184
19	23391206	23391207	C	T	25	GENIC	homozygous	109864467
19	23392409	23392410	A	G	32	GENIC	possibly homozygous	109864473
19	23392411	23392412	A	G	29	GENIC	homozygous	109864475
19	23392611	23392612	A	G	35	GENIC	homozygous	109864477
19	23391683	23391683		C	21	GENIC	possibly homozygous	132763807
19	23393291	23393291		AAACAAAAAAC	34	GENIC	heterozygous	132763808
19	23393343	23393344	G	C	44	GENIC	homozygous	109888072
19	23393599	23393600	C	T	52	GENIC	homozygous	109864479
19	23394715	23394716	A	G	34	GENIC	homozygous	109864482
19	23394767	23394769	GG		31	GENIC	homozygous	132763809
19	23394781	23394781		T	34	GENIC	homozygous	131216934
19	23395058	23395059	C	A	19	GENIC	homozygous	109864484
19	23395806	23395807	A		33	GENIC	possibly homozygous	131216935
19	23395941	23395942	C		49	GENIC	homozygous	131216936
19	23396824	23396825	G	A	23	GENIC	homozygous	109864486
19	23398250	23398252	GT		24	GENIC	homozygous	132763810
19	23398296	23398297	G	A	32	GENIC	homozygous	109864488
19	23398655	23398656	A	G	28	GENIC	homozygous	109864490
19	23399214	23399214		CACCAG	38	GENIC	homozygous	131216937
19	23399331	23399332	T	C	35	GENIC	homozygous	109864492
19	23399373	23399374	C	T	48	GENIC	homozygous	109864494
19	23399388	23399389	A	G	47	GENIC	homozygous	109864496
19	23397827	23397828	T	G	19	GENIC	homozygous	119657723
19	23397834	23397835	C	G	20	GENIC	homozygous	119601806
19	23397841	23397842	C	G	22	GENIC	homozygous	109801718
19	23397854	23397855	T	C	25	GENIC	homozygous	109774895
19	23401476	23401477	A	G	36	GENIC	homozygous	109864498