chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	30686687	30686688	C	T	29	GENIC	homozygous	111023387
17	30687484	30687485	T	C	27	GENIC	homozygous	111023389
17	30687998	30687999	T	C	17	GENIC	homozygous	111023391
17	30688185	30688186	C	G	9	GENIC	homozygous	111023393
17	30691746	30691747	C	G	11	GENIC	homozygous	111023395
17	30692884	30692885	T	G	26	GENIC	homozygous	111023397
17	30694599	30694600	T	C	17	GENIC	homozygous	111023399
17	30694908	30694909	A	G	20	GENIC	homozygous	111023401
17	30694927	30694928	C	T	19	GENIC	homozygous	111023403
17	30696769	30696770	A	G	15	GENIC	homozygous	111499390
17	30698685	30698686	T	G	19	GENIC	homozygous	111023405
17	30700555	30700556	A	G	18	GENIC	homozygous	111023407
17	30701936	30701937	G	T	10	GENIC	possibly homozygous	111023411
17	30702601	30702602	T	C	11	GENIC	homozygous	111023413
17	30702783	30702784	A	G	25	GENIC	homozygous	111023415
17	30702898	30702899	G	A	35	GENIC	homozygous	111023417
17	30703369	30703370	G	A	29	GENIC	homozygous	111023419
17	30706862	30706863	T	C	15	GENIC	homozygous	111023421
17	30708783	30708784	G	T	10	GENIC	homozygous	111023423
17	30709626	30709627	C	T	12	GENIC	homozygous	111023425
17	30709923	30709924	A	G	13	GENIC	homozygous	111023427
17	30711389	30711390	C	T	10	GENIC	homozygous	111023429
17	30712226	30712227	C	T	14	GENIC	homozygous	111023431