chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14303534	14303535	T	C	26	GENIC	homozygous	139089357
12	14304515	14304516	A	G	11	GENIC	homozygous	139089358
12	14304672	14304673	T	C	13	GENIC	homozygous	139089359
12	14304887	14304888	C	T	13	GENIC	homozygous	139089360
12	14305148	14305149	T	C	22	GENIC	homozygous	139089361
12	14305292	14305293	T	C	25	GENIC	homozygous	139089362
12	14305320	14305321	A	G	23	GENIC	homozygous	139089363
12	14306672	14306673	C	T	6	GENIC	homozygous	139089364
12	14306674	14306675	C	T	6	GENIC	homozygous	139089365
12	14306962	14306963	A	T	18	GENIC	homozygous	139089366
12	14307141	14307142	A	G	14	GENIC	homozygous	139089367
12	14307213	14307214	T	C	15	GENIC	homozygous	139089368
12	14308360	14308361	T	G	9	GENIC	homozygous	139089371
12	14308430	14308431	T	C	9	GENIC	homozygous	139089372
12	14308926	14308927	A	G	12	GENIC	homozygous	139089373
12	14309073	14309074	G	A	16	GENIC	homozygous	139089374
12	14309106	14309107	A	G	21	GENIC	homozygous	139089375
12	14308094	14308095	T	C	8	GENIC	homozygous	144921542
12	14306686	14306686		T	9	GENIC	homozygous	139042158
12	14309221	14309222	C		16	GENIC	homozygous	139042159
12	14308075	14308076	A		6	GENIC	homozygous	403317460
12	14308075	14308076	A	G	6	GENIC	heterozygous	403317461
12	14308076	14308077	T		6	GENIC	homozygous	403317462
12	14308076	14308077	T	C	6	GENIC	heterozygous	403317463