chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	190585791	190585792	G	A	20	GENIC	homozygous	109178267
1	190586140	190586141	C	A	17	GENIC	heterozygous	109530285
1	190587876	190587877	G	A	12	GENIC	homozygous	108465706
1	190588459	190588460	G	C	19	GENIC	homozygous	108465707
1	190589874	190589875	A	G	36	GENIC	homozygous	108465709
1	190591839	190591840	G	A	19	GENIC	homozygous	108465710
1	190596155	190596156	A	T	45	GENIC	homozygous	108465712
1	190597825	190597826	T	G	24	GENIC	homozygous	108465714
1	190598462	190598463	T	A	16	GENIC	homozygous	109178269
1	190598463	190598464	C	T	16	GENIC	homozygous	120781658
1	190598881	190598882	T	C	14	GENIC	homozygous	109178271
1	190598960	190598961	T	C	14	GENIC	homozygous	108465715
1	190598964	190598965	C	T	12	GENIC	homozygous	120781659
1	190599019	190599020	C	T	14	GENIC	homozygous	108465716
1	190599318	190599319	C	A	19	GENIC	possibly homozygous	108465717
1	190601531	190601532	C	T	19	GENIC	homozygous	108465718
1	190601782	190601783	A	C	20	GENIC	homozygous	108465719
1	190602553	190602554	C	T	17	GENIC	homozygous	108465720
1	190602709	190602710	G	C	23	GENIC	homozygous	108465721
1	190603902	190603903	G	A	28	GENIC	homozygous	108465722