chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	124517770	124517771	G	C	20	GENIC	homozygous	111694446
3	124519964	124519965	C	A	18	GENIC	possibly homozygous	111694449
3	124521401	124521402	T	C	9	GENIC	homozygous	111694450
3	124521522	124521523	T	C	10	GENIC	homozygous	111694451
3	124521741	124521742	C	T	24	GENIC	homozygous	111694452
3	124522300	124522301	A	G	29	GENIC	homozygous	111694453
3	124522785	124522786	T	C	21	GENIC	homozygous	111694455
3	124523340	124523341	A	T	25	GENIC	homozygous	111694456
3	124523651	124523652	A	G	12	GENIC	homozygous	111694457
3	124523795	124523796	C	T	17	GENIC	homozygous	111694458
3	124524132	124524133	C	A	22	GENIC	homozygous	111694459
3	124525019	124525020	A	G	20	GENIC	homozygous	111694460
3	124525044	124525045	C	T	15	GENIC	homozygous	111694461
3	124525225	124525226	G	A	26	GENIC	homozygous	111694462
3	124526061	124526062	T	C	18	GENIC	homozygous	111694463
3	124526128	124526129	A	C	17	GENIC	homozygous	111694464
3	124526148	124526149	G	A	24	GENIC	homozygous	111694465
3	124526190	124526191	C	T	20	GENIC	homozygous	111694466
3	124528436	124528437	T	C	17	GENIC	homozygous	111694467
3	124530504	124530505	A	T	16	GENIC	homozygous	111694468
3	124531088	124531089	G	A	13	GENIC	homozygous	111694469