chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23754358	23754359	C	T	35	GENIC	possibly homozygous	115691584
12	23755402	23755403	T	C	27	GENIC	homozygous	115285704
12	23755568	23755569	T	C	40	GENIC	heterozygous	118336857
12	23755572	23755573	T	C	38	GENIC	heterozygous	118336858
12	23755620	23755621	C	T	42	GENIC	heterozygous	118301137
12	23755856	23755857	G	A	50	GENIC	possibly homozygous	118336859
12	23757964	23757965	A	G	42	GENIC	homozygous	118336860
12	23758296	23758297	A	G	36	GENIC	homozygous	115285712
12	23758913	23758914	G	A	19	GENIC	heterozygous	118324918
12	23758919	23758920	T	C	19	GENIC	heterozygous	118261861
12	23758929	23758930	G	A	23	GENIC	heterozygous	118261862
12	23758934	23758935	G	A	24	GENIC	heterozygous	118261863
12	23759317	23759318	A	G	44	GENIC	homozygous	115285718
12	23759579	23759580	C	A	41	GENIC	homozygous	115438458
12	23760808	23760809	T	C	39	GENIC	homozygous	115285722
12	23760818	23760819	T	C	32	GENIC	possibly homozygous	115285724
12	23760916	23760917	G	C	35	GENIC	homozygous	115285726
12	23762134	23762135	T	A	42	GENIC	homozygous	118336861
12	23762535	23762536	A	G	41	GENIC	homozygous	115285730
12	23762995	23762996	G	A	25	GENIC	homozygous	118336862
12	23763546	23763547	T	G	36	GENIC	homozygous	118336863
12	23764672	23764673	C	A	15	GENIC	homozygous	118261864
12	23765328	23765329	T	A	30	GENIC	homozygous	118336864
12	23765345	23765346	A	G	30	GENIC	homozygous	115285738
12	23767622	23767623	A	G	36	GENIC	heterozygous	118336865
12	23767633	23767634	T	C	32	GENIC	heterozygous	118336866
12	23767690	23767691	G	A	13	GENIC	homozygous	118336867
12	23768599	23768600	G	A	47	GENIC	homozygous	115368630
12	23769326	23769327	T	C	28	GENIC	possibly homozygous	115285760