chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	205778169	205778173	TTTG		21	GENIC	homozygous	127476431
1	205780823	205780824	A	G	15	GENIC	homozygous	108515513
1	205782782	205782783	A	G	10	GENIC	homozygous	108515514
1	205783066	205783067	T	A	15	GENIC	homozygous	108515515
1	205783216	205783217	T	C	16	GENIC	homozygous	108515516
1	205783831	205783832	A	G	19	GENIC	homozygous	108515517
1	205783841	205783842	G	A	19	GENIC	homozygous	108515518
1	205784212	205784213	A	G	14	GENIC	homozygous	108515519
1	205784348	205784349	T	C	17	GENIC	homozygous	108515520
1	205784700	205784701	A		9	GENIC	homozygous	127476432
1	205784723	205784724	C	A	16	GENIC	homozygous	108515521
1	205785019	205785020	C	G	15	GENIC	homozygous	108515522
1	205785504	205785505	C	T	13	GENIC	homozygous	108515523
1	205785568	205785569	T	C	10	GENIC	homozygous	108515524
1	205785948	205785948		C	16	GENIC	homozygous	127476433
1	205786087	205786088	A	G	23	GENIC	homozygous	108515525
1	205787279	205787309	GCTGTGTCCCTTGTGTAGACAGGCATGCTG		11	GENIC	homozygous	127476434
1	205787562	205787563	C	T	18	GENIC	homozygous	108515527
1	205787607	205787608	A	T	16	GENIC	homozygous	108515528
1	205787622	205787623	G	A	16	GENIC	homozygous	108515529
1	205788631	205788632	T	C	22	GENIC	homozygous	108515530
1	205789330	205789331	T	G	17	GENIC	homozygous	108515531
1	205789682	205789683	G	A	17	GENIC	homozygous	108515532