chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	107517698	107517699	G	T	20	GENIC	homozygous	115471492
6	107517781	107517782	T	C	15	GENIC	homozygous	115471494
6	107517788	107517789	T	A	16	GENIC	homozygous	115471496
6	107517828	107517829	G	A	15	GENIC	possibly homozygous	115471498
6	107517884	107517885	G	C	24	GENIC	homozygous	115471500
6	107518131	107518132	G	A	32	GENIC	homozygous	115471502
6	107518307	107518308	A	G	21	GENIC	homozygous	115471504
6	107518332	107518333	A	G	22	GENIC	homozygous	115471506
6	107518840	107518841	A	G	27	GENIC	homozygous	115471508
6	107518841	107518842	T	C	28	GENIC	homozygous	115471510
6	107518898	107518899	C	T	36	GENIC	homozygous	115471512
6	107518901	107518902	C	T	35	GENIC	homozygous	115471514
6	107518908	107518909	A	G	37	GENIC	homozygous	115471516
6	107519140	107519141	G	A	20	GENIC	homozygous	115471518
6	107519169	107519170	T	C	13	GENIC	homozygous	115471520
6	107519529	107519530	C	T	17	GENIC	possibly homozygous	115471522
6	107519607	107519608	G	A	14	GENIC	homozygous	115471524
6	107519628	107519629	T	C	12	GENIC	homozygous	115471526
6	107520081	107520082	A	G	24	GENIC	homozygous	115471528
6	107520357	107520358	A	C	23	GENIC	homozygous	115471530
6	107520885	107520886	A	G	22	GENIC	homozygous	115471532
6	107520929	107520930	C	T	25	GENIC	homozygous	115471534
6	107521906	107521907	C	T	25	GENIC	homozygous	115471536
6	107521990	107521991	C	G	14	GENIC	homozygous	115471538
6	107522102	107522103	T	G	21	GENIC	possibly homozygous	115471540
6	107522213	107522214	A	T	21	GENIC	homozygous	115471542
6	107522392	107522393	G	C	29	GENIC	homozygous	115471544
6	107522613	107522614	T	C	25	GENIC	homozygous	115471546
6	107522635	107522636	T	G	27	GENIC	homozygous	115471548
6	107522784	107522785	C	G	27	GENIC	heterozygous	115471550