chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39166151	39166151		TGCAGA	22	GENIC	homozygous	128988100
12	39166253	39166253		AT	25	GENIC	possibly homozygous	133765393
12	39166697	39166698	C	A	44	GENIC	possibly homozygous	115324942
12	39167157	39167158	A	G	24	GENIC	homozygous	115324944
12	39167289	39167290	C	G	17	GENIC	homozygous	115494058
12	39167766	39167767	G	A	19	GENIC	homozygous	115324946
12	39168302	39168303	G	A	35	GENIC	homozygous	115324948
12	39169271	39169272	G		25	GENIC	homozygous	128988104
12	39169323	39169324	T	C	24	GENIC	homozygous	118270175
12	39169373	39169374	T	C	23	GENIC	homozygous	118304700
12	39169402	39169403	A	G	25	GENIC	homozygous	118304701
12	39171834	39171835	A	G	30	GENIC	homozygous	115324964
12	39172304	39172305	T	A	27	GENIC	homozygous	115486247
12	39174227	39174228	A		15	GENIC	homozygous	128988106
12	39174698	39174702	AAAG		25	GENIC	homozygous	131493620
12	39174813	39174814	T	C	16	GENIC	homozygous	118270179
12	39183321	39183322	C	G	29	GENIC	homozygous	115324972