chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	71436366	71436367	G	C	39	GENIC	homozygous	111606546
3	71436411	71436412	C	T	33	GENIC	homozygous	111606547
3	71436845	71436846	A	G	24	GENIC	homozygous	111606549
3	71437838	71437839	T	G	27	GENIC	homozygous	111606550
3	71444302	71444303	A	T	26	GENIC	homozygous	111606553
3	71444917	71444918	A	G	36	GENIC	homozygous	111606554
3	71444948	71444949	A	G	38	GENIC	homozygous	112386637
3	71445944	71445945	A	T	26	GENIC	homozygous	111922087
3	71447080	71447081	T	A	22	GENIC	homozygous	111922089
3	71447457	71447458	G	T	14	GENIC	homozygous	111606555
3	71447467	71447468	A	T	14	GENIC	homozygous	111606556
3	71448031	71448032	T	G	10	GENIC	homozygous	111606557
3	71450299	71450300	T	G	26	GENIC	homozygous	111922101
3	71443386	71443387	C	T	26	GENIC	homozygous	119974800
3	71446299	71446300	G	A	23	GENIC	homozygous	119974801
3	71446678	71446679	G	A	26	GENIC	homozygous	119974802