chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40382238	40382239	T	C	40	GENIC	homozygous	115383570
12	40383528	40383529	G	C	28	GENIC	homozygous	115328073
12	40383623	40383624	T	G	33	GENIC	homozygous	115328075
12	40383749	40383750	T	G	4	GENIC	homozygous	115441476
12	40384089	40384090	C	A	12	GENIC	homozygous	118304969
12	40392006	40392007	C	T	27	GENIC	homozygous	115383572
12	40395560	40395561	T	A	15	GENIC	homozygous	115583191
12	40397358	40397359	C	T	24	GENIC	homozygous	115583193
12	40397599	40397600	T	C	28	GENIC	homozygous	115383574
12	40400186	40400187	A	G	28	GENIC	homozygous	118304971
12	40400213	40400214	A	G	29	GENIC	possibly homozygous	118304972
12	40400238	40400239	A	T	34	GENIC	homozygous	118304973
12	40402137	40402138	T	C	28	GENIC	homozygous	115383576
12	40402326	40402327	C	T	23	GENIC	homozygous	115383578
12	40404119	40404120	T	C	33	GENIC	homozygous	115328079
12	40404128	40404129	A	G	38	GENIC	homozygous	115328081
12	40407681	40407682	T	C	18	GENIC	homozygous	115383584
12	40409093	40409094	T	G	19	GENIC	homozygous	115383586
12	40409437	40409438	G	C	13	GENIC	homozygous	118270521
12	40409457	40409458	G	T	12	GENIC	homozygous	118270522
12	40414069	40414070	C	A	25	GENIC	possibly homozygous	118270523