chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11200252	11200253	A	T	11	GENIC	heterozygous	118244396
12	11200297	11200298	G	A	7	GENIC	heterozygous	118244397
12	11200404	11200405	C	T	5	GENIC	heterozygous	118291898
12	11201918	11201919	C	T	22	GENIC	homozygous	115254782
12	11201950	11201951	A	G	13	GENIC	homozygous	115254784
12	11202205	11202206	T	C	15	GENIC	homozygous	115254788
12	11202310	11202311	A	G	16	GENIC	heterozygous	115254790
12	11202578	11202579	A	G	8	GENIC	heterozygous	118291900
12	11203167	11203168	T	C	19	GENIC	homozygous	115254792
12	11204493	11204494	A	G	12	GENIC	homozygous	115254794
12	11204642	11204643	A	G	14	GENIC	homozygous	115254796
12	11204728	11204729	A	G	14	GENIC	homozygous	115254798
12	11204741	11204742	T	C	17	GENIC	homozygous	115254800
12	11205217	11205218	T	G	28	GENIC	homozygous	115254802
12	11205522	11205523	T	C	11	GENIC	homozygous	115415268
12	11202209	11202210	G	A	7	GENIC	homozygous	115415264
12	11203424	11203425	T	G	21	GENIC	homozygous	115415266
12	11205636	11205637	T	G	24	GENIC	homozygous	115254804
12	11206983	11206984	T	C	23	GENIC	homozygous	115254808
12	11207617	11207618	C	T	26	GENIC	homozygous	115415270
12	11207912	11207913	C	T	20	GENIC	homozygous	115254812
12	11208642	11208643	C	T	31	GENIC	homozygous	115254816
12	11208717	11208718	T	C	17	GENIC	homozygous	115254818
12	11208742	11208743	T	C	18	GENIC	homozygous	115254820
12	11209532	11209533	T	C	20	GENIC	homozygous	115254824
12	11209657	11209658	T	C	22	GENIC	homozygous	115254826
12	11211493	11211494	G	T	17	GENIC	homozygous	115254834
12	11211987	11211988	C	G	24	GENIC	possibly homozygous	115415274
12	11212326	11212327	A	G	20	GENIC	homozygous	115254844
12	11212410	11212411	C	T	24	GENIC	homozygous	115254846
12	11213338	11213339	T	C	26	GENIC	homozygous	115415276
12	11213714	11213715	T	C	8	GENIC	homozygous	115415278
12	11213715	11213716	G	A	8	GENIC	homozygous	115415280