chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41409333	41409334	T	C	14	GENIC	homozygous	115330196
12	41409448	41409449	G	A	18	GENIC	homozygous	115330198
12	41410024	41410025	C	A	15	GENIC	homozygous	115330200
12	41410054	41410055	C	T	10	GENIC	homozygous	115330202
12	41410329	41410330	C	T	8	GENIC	homozygous	115330204
12	41410985	41410986	C	T	6	GENIC	homozygous	115385205
12	41411255	41411256	T	G	20	GENIC	homozygous	115330206
12	41411299	41411300	G	A	20	GENIC	homozygous	115330208
12	41411688	41411689	C	G	22	GENIC	homozygous	115330210
12	41411734	41411735	A	G	18	GENIC	homozygous	115330212
12	41412087	41412088	A	G	21	GENIC	homozygous	115330214
12	41412107	41412108	T	G	24	GENIC	homozygous	115330216
12	41414307	41414308	G	A	21	GENIC	homozygous	115330220
12	41414507	41414508	C	T	18	GENIC	homozygous	115330222
12	41414942	41414943	A	C	16	GENIC	homozygous	115330224
12	41415197	41415198	G	T	7	GENIC	homozygous	126173584