chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19009331	19009332	T		40	GENIC	heterozygous	128968219
12	19010954	19010955	C	T	30	GENIC	heterozygous	129009040
12	19010965	19010966	G	C	25	GENIC	heterozygous	129009041
12	19011013	19011014	C	A	26	GENIC	heterozygous	129009042
12	19011044	19011045	G	T	30	GENIC	heterozygous	129009044
12	19011396	19011397	A	G	20	GENIC	heterozygous	129009048
12	19012123	19012124	C	T	43	GENIC	heterozygous	118340762
12	19011871	19011872	T	G	17	GENIC	heterozygous	131721838
12	19011879	19011880	C	A	20	GENIC	heterozygous	131721839
12	19012505	19012506	G	T	67	GENIC	heterozygous	118247426
12	19012579	19012580	G	A	31	GENIC	heterozygous	118323126
12	19012600	19012601	G	A	24	GENIC	heterozygous	118378054
12	19012653	19012654	A	G	30	GENIC	heterozygous	133429411
12	19012794	19012795	G	A	21	GENIC	heterozygous	132168870
12	19013010	19013011	G	T	36	GENIC	heterozygous	131721840
12	19013219	19013220	A		73	GENIC	heterozygous	131720062
12	19013232	19013233	C	T	77	GENIC	heterozygous	118323129
12	19013800	19013801	C		51	GENIC	heterozygous	131720063
12	19014110	19014111	C	T	25	GENIC	heterozygous	131721841
12	19014442	19014443	C	T	50	GENIC	heterozygous	118340763
12	19014931	19014932	T	C	40	GENIC	heterozygous	133429413
12	19014932	19014933	A	T	41	GENIC	heterozygous	133429414
12	19014999	19015000	C	A	35	GENIC	heterozygous	118340765
12	19015118	19015119	T	C	40	GENIC	heterozygous	118323150
12	19015191	19015192	C	A	38	GENIC	heterozygous	118340766
12	19015202	19015203	T	A	39	GENIC	heterozygous	118340767