chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	83951397	83951398	C	T	34	GENIC	homozygous	115998013
11	83951755	83951756	T	C	25	GENIC	homozygous	115998015
11	83952809	83952810	C	T	28	GENIC	homozygous	115998017
11	83953068	83953069	A	G	31	GENIC	homozygous	115998019
11	83953211	83953212	A	C	19	GENIC	homozygous	115998021
11	83955759	83955760	C	T	38	GENIC	homozygous	115998023
11	83955841	83955842	G	A	36	GENIC	homozygous	115998025
11	83956628	83956629	C	G	21	GENIC	homozygous	115998027
11	83958788	83958789	A	C	19	GENIC	homozygous	116162563
11	83960043	83960044	T	A	27	GENIC	homozygous	115998031
11	83961000	83961001	G	A	11	GENIC	homozygous	115998033
11	83961137	83961138	A	T	22	GENIC	homozygous	115998035
11	83961534	83961535	T	A	35	GENIC	homozygous	115998037
11	83962916	83962917	C	T	17	GENIC	homozygous	115998039
11	83972074	83972075	A	G	31	GENIC	homozygous	115998041
11	83972381	83972382	T	A	29	GENIC	homozygous	115998043