chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39873586	39873587	C	T	27	GENIC	possibly homozygous	50201963
12	39873684	39873685	T	C	27	GENIC	possibly homozygous	50201965
12	39874325	39874327	TC	--	10	GENIC	homozygous	50201967
12	39874389	39874390	A	G	24	GENIC	possibly homozygous	50201969
12	39874588	39874589	C	T	26	GENIC	homozygous	50201971
12	39874992	39874993	G	A	21	GENIC	homozygous	50201973
12	39875037	39875039	GT	--	5	GENIC	heterozygous	50201975
12	39875350	39875351	G	GTC	4	GENIC	heterozygous	50201989
12	39875397	39875398	A	G	12	GENIC	heterozygous	50201993
12	39875512	39875514	TA	--	3	GENIC	homozygous	50201997
12	39875809	39875810	C	T	20	GENIC	homozygous	50201999
12	39877253	39877254	A	-	2	GENIC	heterozygous	50380996
12	39877765	39877766	G	-	4	GENIC	homozygous	50512107
12	39878414	39878418	ACAC	----	2	GENIC	heterozygous	50452073
12	39879212	39879213	G	A	20	GENIC	possibly homozygous	50202021
12	39879495	39879496	A	G	8	GENIC	homozygous	50202023
12	39880710	39880711	C	-	17	GENIC	possibly homozygous	50202027
12	39881345	39881346	A	G	30	GENIC	possibly homozygous	50202028
12	39881481	39881482	C	G	15	GENIC	homozygous	50202030