chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11240779	11240780	C	T	11	GENIC	homozygous	115620825
12	11241390	11241391	A	C	37	GENIC	possibly homozygous	115594771
12	11243043	11243044	G	A	28	GENIC	homozygous	115415351
12	11243054	11243055	A	C	30	GENIC	homozygous	115415353
12	11243204	11243205	C	A	29	GENIC	homozygous	115594773
12	11243893	11243894	T	G	23	GENIC	homozygous	115254912
12	11243921	11243922	T	G	24	GENIC	homozygous	115415355
12	11244353	11244354	T	C	21	GENIC	homozygous	115415357
12	11244425	11244426	C	A	19	GENIC	homozygous	115415359
12	11244565	11244566	C	T	26	GENIC	possibly homozygous	115415363
12	11244773	11244774	T	C	24	GENIC	homozygous	115445087
12	11244780	11244781	A	G	25	GENIC	homozygous	115254914
12	11244867	11244868	T	C	20	GENIC	possibly homozygous	115415367
12	11245545	11245546	C	T	21	GENIC	homozygous	115415371
12	11245623	11245624	A	G	25	GENIC	homozygous	115415373
12	11245819	11245820	A	T	35	GENIC	homozygous	115415375
12	11246311	11246312	T	A	17	GENIC	possibly homozygous	115594775
12	11246821	11246822	G	A	28	GENIC	homozygous	115254916
12	11247364	11247365	T	A	31	GENIC	homozygous	115594777
12	11248580	11248581	A	G	18	GENIC	homozygous	115415379
12	11249902	11249903	A	T	22	GENIC	homozygous	115415381