chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44280798	44280799	T	C	10	GENIC	homozygous	109723321
2	44282495	44282496	G	A	26	GENIC	homozygous	120167143
2	44282572	44282573	T	C	13	GENIC	homozygous	109723325
2	44283721	44283722	C	G	15	GENIC	homozygous	120167144
2	44290651	44290652	G	A	10	GENIC	homozygous	120167145
2	44296074	44296075	G	A	16	GENIC	homozygous	120167146
2	44296094	44296095	A	G	11	GENIC	homozygous	109723353
2	44301705	44301706	A	C	9	GENIC	homozygous	120123640
2	44306264	44306265	C	T	13	GENIC	homozygous	109723375
2	44306747	44306748	A	G	16	GENIC	homozygous	109723377
2	44309534	44309535	A	G	13	GENIC	homozygous	109723379
2	44311438	44311439	C	T	19	GENIC	homozygous	110507355
2	44313672	44313673	C	T	18	GENIC	homozygous	120167147
2	44316750	44316751	C	T	13	GENIC	homozygous	109723395
2	44317976	44317977	A	G	19	GENIC	homozygous	109723397