chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18013994	18013995	A	G	24	GENIC	heterozygous	50506883
12	18014115	18014117	CA	--	33	GENIC	heterozygous	50506885
12	18014830	18014831	T	C	45	GENIC	heterozygous	50506887
12	18014959	18014960	G	A	45	GENIC	heterozygous	50506889
12	18014968	18014969	T	C	47	GENIC	heterozygous	50506891
12	18015867	18015868	T	TG	33	GENIC	heterozygous	50506901
12	18016325	18016326	T	A	28	GENIC	heterozygous	50506903
12	18016345	18016346	G	A	34	GENIC	heterozygous	50506905
12	18018112	18018113	C	T	23	GENIC	heterozygous	50506921
12	18018183	18018184	G	A	21	GENIC	heterozygous	50506923
12	18018339	18018340	G	A	27	GENIC	heterozygous	50506925
12	18018347	18018348	G	A	25	GENIC	heterozygous	50506927
12	18018363	18018364	A	G	18	GENIC	heterozygous	50506929
12	18018527	18018528	C	T	14	GENIC	heterozygous	50506931
12	18020284	18020285	A	G	22	GENIC	heterozygous	50089211
12	18022578	18022579	A	C	34	GENIC	heterozygous	50506951
12	18035627	18035628	G	A	29	GENIC	heterozygous	50506959