chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40382122	40382123	C	T	25	GENIC	homozygous	115441475
12	40383368	40383369	G	T	25	GENIC	possibly homozygous	115451437
12	40383528	40383529	G	C	26	GENIC	homozygous	115328073
12	40383623	40383624	T	G	22	GENIC	homozygous	115328075
12	40383749	40383750	T	G	4	GENIC	homozygous	115441476
12	40397599	40397600	T	C	19	GENIC	homozygous	115383574
12	40398341	40398342	T	C	15	GENIC	homozygous	115441477
12	40398344	40398345	T	C	15	GENIC	homozygous	115441478
12	40400213	40400214	A	G	20	GENIC	homozygous	118304972
12	40400239	40400240	C	T	21	GENIC	possibly homozygous	118326981
12	40402137	40402138	T	C	21	GENIC	homozygous	115383576
12	40402326	40402327	C	T	36	GENIC	homozygous	115383578
12	40404119	40404120	T	C	15	GENIC	homozygous	115328079
12	40404128	40404129	A	G	14	GENIC	homozygous	115328081
12	40407681	40407682	T	C	9	GENIC	homozygous	115383584
12	40409093	40409094	T	G	28	GENIC	homozygous	115383586
12	40409457	40409458	G	T	9	GENIC	homozygous	118270522
12	40402785	40402786	C	T	3	GENIC	homozygous	118270519
12	40405173	40405174	T	C	10	GENIC	possibly homozygous	118270520
12	40409437	40409438	G	C	9	GENIC	homozygous	118270521
12	40414069	40414070	C	A	12	GENIC	heterozygous	118270523