chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	49905424	49905425	T	A	35	GENIC	homozygous	964061210
6	49905429	49905430	C	A	35	GENIC	homozygous	964061211
6	49905700	49905701	A	G	27	GENIC	homozygous	964061212
6	49906569	49906570	C	T	3	GENIC	homozygous	964061213
6	49906574	49906575	T	C	2	GENIC	homozygous	964061214
6	49906933	49906934	G	C	6	GENIC	homozygous	964061215
6	49906990	49906991	T	C	21	GENIC	homozygous	964061216
6	49907003	49907004	C	G	25	GENIC	homozygous	964061217
6	49907383	49907384	A	G	31	GENIC	homozygous	964061218
6	49907621	49907622	T	C	24	GENIC	homozygous	964061219
6	49907702	49907703	T	C	25	GENIC	homozygous	964061220
6	49907907	49907908	T	C	19	GENIC	homozygous	964061221
6	49908105	49908106	A	T	19	GENIC	homozygous	964061222
6	49908219	49908220	G	A	17	GENIC	homozygous	964061223
6	49908578	49908579	G	A	25	GENIC	homozygous	964061224
6	49909099	49909100	C	T	35	GENIC	homozygous	964061225
6	49909501	49909502	T	C	34	GENIC	homozygous	964061226
6	49909548	49909549	C	A	27	GENIC	homozygous	964061227
6	49909587	49909588	G	A	23	GENIC	homozygous	964061228
6	49910176	49910177	C	T	20	GENIC	homozygous	964061229
6	49910203	49910204	C	T	19	GENIC	homozygous	964061230