chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	62155020	62155021	A	G	24	GENIC	homozygous	109786424
2	62160634	62160635	A	G	23	GENIC	homozygous	109786446
2	62161251	62161252	G	T	24	GENIC	homozygous	109786452
2	62169326	62169327	T	A	20	GENIC	homozygous	109786486
2	62171859	62171860	A	G	16	GENIC	homozygous	109786494
2	62172233	62172234	A	G	25	GENIC	homozygous	109786498
2	62159938	62159939	T	G	23	GENIC	homozygous	120360115
2	62160454	62160455	C	T	22	GENIC	possibly homozygous	120360116
2	62161380	62161381	T	C	25	GENIC	possibly homozygous	120360117
2	62171706	62171707	G	A	18	GENIC	homozygous	120360118
2	62176809	62176810	G	T	12	GENIC	homozygous	109786517
2	62177625	62177626	C	T	32	GENIC	homozygous	109786521
2	62180956	62180957	A	C	31	GENIC	possibly homozygous	120360120
2	62182685	62182686	A	C	12	GENIC	homozygous	120360122
2	62183386	62183387	C	T	23	GENIC	homozygous	120360123
2	62185069	62185070	T	C	19	GENIC	homozygous	109786547
2	62189656	62189657	T	C	23	GENIC	homozygous	120360124
2	62190787	62190788	A	C	28	GENIC	homozygous	109786571
2	62191140	62191141	T	C	29	GENIC	homozygous	109786573
2	62193144	62193145	T	C	25	GENIC	homozygous	109786575
2	62194115	62194116	C	T	20	GENIC	possibly homozygous	120360125
2	62195620	62195621	G	A	28	GENIC	possibly homozygous	120360126
2	62198245	62198246	A	G	25	GENIC	homozygous	109786579
2	62200538	62200539	C	T	34	GENIC	homozygous	109786583
2	62201820	62201821	A	G	22	GENIC	possibly homozygous	109786585
2	62206488	62206489	C	T	26	GENIC	homozygous	109786589
2	62207694	62207695	A	T	22	GENIC	possibly homozygous	109786591
2	62211228	62211229	G	A	34	GENIC	possibly homozygous	120360127
2	62211542	62211543	A	G	25	GENIC	homozygous	109786595