chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	34472297	34472298	G	C	24	GENIC	homozygous	190618596
12	34472874	34472875	A	G	15	GENIC	homozygous	188665239
12	34473652	34473653	C	T	26	GENIC	homozygous	188665240
12	34476190	34476191	G	A	35	GENIC	homozygous	188665241
12	34477351	34477352	G	T	14	GENIC	homozygous	190618597
12	34478158	34478159	A	G	14	GENIC	homozygous	190618598
12	34478220	34478221	C	T	10	GENIC	homozygous	190618599
12	34480755	34480756	T	C	16	GENIC	homozygous	190618600
12	34481027	34481028	C	A	9	GENIC	possibly homozygous	190618601
12	34481028	34481029	A	C	9	GENIC	possibly homozygous	190618602
12	34481586	34481587	A	G	10	GENIC	homozygous	188665242
12	34481877	34481878	A	G	21	GENIC	homozygous	188665243
12	34482888	34482889	T	G	9	GENIC	homozygous	190618603
12	34486529	34486530	A	G	8	GENIC	homozygous	188665244
12	34488042	34488043	C	G	6	GENIC	homozygous	190618604
12	34490791	34490792	G	T	27	GENIC	homozygous	188665245
12	34494012	34494013	G	T	23	GENIC	homozygous	188665246
12	34494064	34494065	A	G	24	GENIC	homozygous	188665247
12	34495097	34495098	A	G	7	GENIC	heterozygous	190618605
12	34496018	34496019	C	T	9	GENIC	homozygous	190618606
12	34497175	34497176	A	G	29	GENIC	homozygous	190618607
12	34499735	34499736	C	T	24	GENIC	homozygous	190618608
12	34500442	34500443	T	C	19	GENIC	homozygous	188665248