chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23753892	23753893	C	A	40	GENIC	homozygous	115368610
12	23754546	23754547	A	G	16	GENIC	homozygous	115469740
12	23755402	23755403	T	C	36	GENIC	homozygous	115285704
12	23755711	23755712	C	T	25	GENIC	homozygous	115368612
12	23756656	23756657	T	C	31	GENIC	homozygous	115285710
12	23758296	23758297	A	G	27	GENIC	homozygous	115285712
12	23758424	23758425	C	T	43	GENIC	homozygous	115368614
12	23758631	23758632	T	C	26	GENIC	homozygous	115285716
12	23759079	23759080	C	T	36	GENIC	homozygous	115368616
12	23759672	23759673	G	A	27	GENIC	homozygous	115368618
12	23760808	23760809	T	C	14	GENIC	homozygous	115285722
12	23760818	23760819	T	C	14	GENIC	homozygous	115285724
12	23760916	23760917	G	C	15	GENIC	homozygous	115285726
12	23762535	23762536	A	G	30	GENIC	homozygous	115285730
12	23762999	23763000	G	A	27	GENIC	homozygous	115368624
12	23764872	23764873	A	G	22	GENIC	homozygous	115368626
12	23768599	23768600	G	A	29	GENIC	homozygous	115368630
12	23768717	23768718	C	T	29	GENIC	homozygous	115368632
12	23769326	23769327	T	C	25	GENIC	homozygous	115285760