chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39873850	39873851	T	C	24	GENIC	homozygous	50380988
12	39874325	39874327	TC	--	22	GENIC	homozygous	50201967
12	39874389	39874390	A	G	15	GENIC	homozygous	50201969
12	39874588	39874589	C	T	23	GENIC	homozygous	50201971
12	39874992	39874993	G	A	37	GENIC	homozygous	50201973
12	39875037	39875039	GT	--	33	GENIC	homozygous	50201975
12	39875350	39875351	G	GTC	40	GENIC	possibly homozygous	50201989
12	39875397	39875398	A	G	43	GENIC	homozygous	50201993
12	39875512	39875514	TA	--	36	GENIC	homozygous	50201997
12	39875809	39875810	C	T	24	GENIC	homozygous	50201999
12	39875989	39875991	AA	--	17	GENIC	heterozygous	50323165
12	39875990	39875991	A	-	17	GENIC	heterozygous	50202005
12	39876414	39876415	G	A	11	GENIC	homozygous	50421941
12	39877765	39877766	G	-	15	GENIC	possibly homozygous	50512107
12	39878253	39878254	C	CAAAAAAAAA	3	GENIC	heterozygous	50558948
12	39878275	39878276	A	-	8	GENIC	homozygous	50202013
12	39878413	39878414	T	TAC	11	GENIC	possibly homozygous	50202015
12	39878609	39878611	AA	--	2	GENIC	homozygous	50543397
12	39879212	39879213	G	A	18	GENIC	homozygous	50202021
12	39879495	39879496	A	G	10	GENIC	homozygous	50202023
12	39880710	39880711	C	-	26	GENIC	homozygous	50202027
12	39881481	39881482	C	G	19	GENIC	homozygous	50202030