chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2069704	2069705	C	T	20	GENIC	homozygous	126162459
12	2070042	2070043	A	G	25	GENIC	homozygous	126162460
12	2070536	2070537	T	C	6	GENIC	homozygous	126162461
12	2071645	2071646	C	G	11	GENIC	heterozygous	126162462
12	2071698	2071699	C	T	22	GENIC	homozygous	126162463
12	2071898	2071899	A	G	18	GENIC	homozygous	126162464
12	2072115	2072116	A	G	6	GENIC	homozygous	126162465
12	2072428	2072429	G	T	10	GENIC	homozygous	126162466
12	2072445	2072446	G	T	6	GENIC	homozygous	126162467
12	2072535	2072536	G	T	19	GENIC	homozygous	126162468
12	2072897	2072898	A	C	23	GENIC	homozygous	126162469
12	2073355	2073356	C	G	22	GENIC	homozygous	126162470
12	2073662	2073663	G	T	24	GENIC	homozygous	126162471
12	2073737	2073738	A	G	28	GENIC	homozygous	126162472
12	2073795	2073796	A	G	28	GENIC	homozygous	126162473
12	2075126	2075127	C	A	24	GENIC	homozygous	126162474
12	2075262	2075263	C	T	12	GENIC	homozygous	126162475
12	2077455	2077456	A	T	11	GENIC	homozygous	126162476
12	2085077	2085078	T	A	10	GENIC	homozygous	126162477
12	2089789	2089790	T	C	8	GENIC	homozygous	126162478
12	2093371	2093372	G	A	16	GENIC	homozygous	126162479
12	2094817	2094818	C	T	5	GENIC	homozygous	126162480
12	2096894	2096895	C	T	11	GENIC	homozygous	126162481