chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13970151	13970152	A	G	24	GENIC	homozygous	115261867
12	13971412	13971413	A	C	11	GENIC	homozygous	115261873
12	13972563	13972564	T	G	18	GENIC	homozygous	115261877
12	13972764	13972765	A	C	24	GENIC	homozygous	115261879
12	13974156	13974157	C	T	19	GENIC	homozygous	115261881
12	13975368	13975369	A	G	19	GENIC	homozygous	115261893
12	13980731	13980732	T	C	28	GENIC	homozygous	115261911
12	13980439	13980440	T	C	30	GENIC	homozygous	115261909
12	13979545	13979546	G	T	15	GENIC	homozygous	115595454
12	13980128	13980129	T	G	31	GENIC	possibly homozygous	115595456
12	13981691	13981692	C	T	28	GENIC	possibly homozygous	115595458
12	13981752	13981753	C	T	21	GENIC	homozygous	115261913
12	13984608	13984609	C	A	29	GENIC	homozygous	115261915
12	13985055	13985056	T	C	25	GENIC	homozygous	115261917
12	13985589	13985590	A	G	27	GENIC	homozygous	115362896
12	13986173	13986174	T	G	36	GENIC	homozygous	115261921
12	13986254	13986255	C	T	43	GENIC	homozygous	115537484
12	13987907	13987908	G	A	31	GENIC	homozygous	115595460
12	13988856	13988857	T	C	31	GENIC	homozygous	115261925
12	13988887	13988888	G	A	34	GENIC	possibly homozygous	115595462
12	13991791	13991792	G	A	28	GENIC	homozygous	115595466
12	13992685	13992686	T	C	22	GENIC	homozygous	115261929
12	13992986	13992987	G	A	24	GENIC	homozygous	115595468
12	13993404	13993405	A	T	30	GENIC	homozygous	115261935
12	13994104	13994105	T	A	27	GENIC	possibly homozygous	115595470
12	13996475	13996476	G	A	24	GENIC	homozygous	115595472
12	13997548	13997549	A	G	27	GENIC	possibly homozygous	115261961
12	13997696	13997697	A	G	19	GENIC	possibly homozygous	115261963