chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40382238	40382239	T	C	9	GENIC	homozygous	115383570
12	40383281	40383282	C	A	14	GENIC	homozygous	115328067
12	40383408	40383409	C	T	5	GENIC	homozygous	115328069
12	40383409	40383410	T	C	5	GENIC	homozygous	115328071
12	40392006	40392007	C	T	26	GENIC	homozygous	115383572
12	40397599	40397600	T	C	14	GENIC	homozygous	115383574
12	40402137	40402138	T	C	10	GENIC	homozygous	115383576
12	40402326	40402327	C	T	14	GENIC	homozygous	115383578
12	40404119	40404120	T	C	13	GENIC	homozygous	115328079
12	40404128	40404129	A	G	13	GENIC	homozygous	115328081
12	40404618	40404619	T	A	12	GENIC	homozygous	115383580
12	40404623	40404624	A	T	7	GENIC	homozygous	115383582
12	40407681	40407682	T	C	4	GENIC	homozygous	115383584
12	40409093	40409094	T	G	17	GENIC	homozygous	115383586
12	40417352	40417353	T	C	4	GENIC	heterozygous	115494856