chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51878381	51878382	T	C	10	GENIC	homozygous	115355708
12	51879559	51879560	A	G	16	GENIC	homozygous	115355709
12	51879874	51879875	A	G	21	GENIC	homozygous	115355710
12	51881039	51881040	C	A	22	GENIC	homozygous	115355711
12	51881124	51881125	G	C	26	GENIC	homozygous	115355712
12	51882232	51882233	T	C	10	GENIC	homozygous	115355713
12	51882265	51882266	G	A	5	GENIC	homozygous	115355714
12	51882449	51882450	G	A	8	GENIC	homozygous	115355715
12	51883037	51883038	T	C	18	GENIC	heterozygous	115430746
12	51883760	51883761	G	A	26	GENIC	homozygous	115355716
12	51884005	51884006	T	C	7	GENIC	heterozygous	115704756
12	51884871	51884872	A	G	15	GENIC	homozygous	115355717
12	51885584	51885585	A	G	22	GENIC	homozygous	126175799
12	51885673	51885674	A	C	12	GENIC	homozygous	126175800
12	51885674	51885675	A	G	13	GENIC	homozygous	126175801
12	51885746	51885747	A	G	12	GENIC	homozygous	126175802
12	51885948	51885949	T	G	23	GENIC	homozygous	126175804
12	51887070	51887071	G	A	8	GENIC	homozygous	115355718
12	51887116	51887117	G	A	4	GENIC	homozygous	115355719
12	51887622	51887623	G	A	18	GENIC	homozygous	115355720
12	51888085	51888086	A	G	20	GENIC	homozygous	115521780