chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19600020	19600021	T	C	16	GENIC	homozygous	115279489
12	19601616	19601617	A	G	20	GENIC	homozygous	115279495
12	19602390	19602391	G	A	11	GENIC	homozygous	115279497
12	19605730	19605731	A	G	6	GENIC	homozygous	115366040
12	19606467	19606468	T	C	13	GENIC	homozygous	115279499
12	19608037	19608038	G	A	16	GENIC	homozygous	115279501
12	19608936	19608937	C	A	23	GENIC	homozygous	115366042
12	19609025	19609026	G	T	23	GENIC	homozygous	115279509
12	19609491	19609492	C	T	27	GENIC	homozygous	115366044
12	19610010	19610011	G	A	15	GENIC	homozygous	115279511
12	19616541	19616542	T	C	22	GENIC	homozygous	115279515
12	19618778	19618779	G	A	23	GENIC	homozygous	115279517
12	19619483	19619484	T	C	24	GENIC	homozygous	115279519
12	19620322	19620323	C	T	20	GENIC	homozygous	118248761
12	19625325	19625326	C	T	18	GENIC	homozygous	118248762
12	19626240	19626241	T	C	10	GENIC	homozygous	115279521
12	19627588	19627589	G	A	19	GENIC	homozygous	115279527
12	19627881	19627882	T	G	20	GENIC	homozygous	115279529
12	19629185	19629186	A	G	20	GENIC	homozygous	115279531
12	19627775	19627776	C	A	5	GENIC	heterozygous	126220850