chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	49969697	49969698	G	T	26	GENIC	homozygous	115109766
6	49969839	49969840	A	T	24	GENIC	homozygous	115109767
6	49970036	49970037	G	T	22	GENIC	heterozygous	115109768
6	49970243	49970244	G	A	22	GENIC	homozygous	115109769
6	49970325	49970326	G	A	27	GENIC	homozygous	114796314
6	49970702	49970703	A	G	25	GENIC	homozygous	114796315
6	49970984	49970985	C	T	20	GENIC	homozygous	115109770
6	49971224	49971225	T	C	23	GENIC	homozygous	115109771
6	49971230	49971231	G	T	22	GENIC	homozygous	115109772
6	49971316	49971317	G	A	22	GENIC	homozygous	115109773
6	49971344	49971345	C	A	22	GENIC	homozygous	115109774
6	49971457	49971458	G	A	28	GENIC	homozygous	115109775
6	49971540	49971541	T	C	19	GENIC	homozygous	115109776
6	49971623	49971624	A	G	19	GENIC	homozygous	115109777
6	49971668	49971669	T	C	18	GENIC	homozygous	115109778
6	49971770	49971771	A	G	13	GENIC	homozygous	115109779
6	49971893	49971894	G	A	18	GENIC	homozygous	115109780
6	49973079	49973080	A	G	25	GENIC	homozygous	114796320
6	49973674	49973675	C	T	25	GENIC	homozygous	115109781
6	49973981	49973982	A	G	20	GENIC	homozygous	114796323
6	49974118	49974119	A	C	21	GENIC	homozygous	114796324
6	49974293	49974294	T	A	26	GENIC	homozygous	114796325