chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	215044118	215044119	A	T	25	GENIC	homozygous	108533401
1	215048235	215048236	T	A	26	GENIC	homozygous	109192092
1	215048482	215048483	C	T	28	GENIC	homozygous	109192094
1	215048560	215048561	C	T	27	GENIC	homozygous	109192096
1	215055901	215055902	G	A	20	GENIC	homozygous	109192100
1	215058632	215058633	A	G	41	GENIC	homozygous	109192102
1	215066872	215066873	A	G	37	GENIC	homozygous	108533419
1	215066971	215066972	A	G	35	GENIC	homozygous	108533421
1	215069585	215069586	T	G	11	GENIC	homozygous	108533425
1	215070766	215070767	C	T	32	GENIC	homozygous	120822077
1	215070768	215070769	T	C	32	GENIC	homozygous	120822078
1	215070956	215070957	C	T	25	GENIC	homozygous	120475846
1	215072038	215072039	A	G	38	GENIC	homozygous	108533442
1	215074866	215074867	G	A	35	GENIC	homozygous	109192104
1	215075927	215075928	G	T	24	GENIC	homozygous	108533443
1	215077079	215077080	T	C	31	GENIC	homozygous	108533444
1	215077900	215077901	A	G	19	GENIC	homozygous	109192106
1	215078673	215078674	C	T	16	GENIC	homozygous	109192108
1	215079568	215079569	G	C	22	GENIC	homozygous	109192110
1	215098358	215098359	G	C	17	GENIC	homozygous	109192112
1	215099469	215099470	C	T	17	GENIC	homozygous	109192114
1	215101155	215101156	C	T	35	GENIC	homozygous	109192120
1	215102908	215102909	C	T	30	GENIC	homozygous	108533470
1	215103130	215103131	T	C	38	GENIC	homozygous	108533471