chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	30683177	30683178	A	G	19	GENIC	homozygous	111317255
17	30687484	30687485	T	C	34	GENIC	possibly homozygous	111023389
17	30687998	30687999	T	C	13	GENIC	homozygous	111023391
17	30688824	30688825	A	G	10	GENIC	heterozygous	111386644
17	30691658	30691659	C	T	18	GENIC	homozygous	111317257
17	30691746	30691747	C	G	19	GENIC	homozygous	111023395
17	30692884	30692885	T	G	27	GENIC	homozygous	111023397
17	30694599	30694600	T	C	26	GENIC	homozygous	111023399
17	30694908	30694909	A	G	29	GENIC	homozygous	111023401
17	30697284	30697285	T	C	16	GENIC	homozygous	111317259
17	30698685	30698686	T	G	14	GENIC	homozygous	111023405
17	30700555	30700556	A	G	17	GENIC	homozygous	111023407
17	30701119	30701120	G	A	38	GENIC	homozygous	111317261
17	30701532	30701533	T	A	17	GENIC	homozygous	111023409
17	30702601	30702602	T	C	21	GENIC	homozygous	111023413
17	30703369	30703370	G	A	24	GENIC	homozygous	111023419
17	30706862	30706863	T	C	26	GENIC	homozygous	111023421
17	30708783	30708784	G	T	24	GENIC	homozygous	111023423
17	30709626	30709627	C	T	17	GENIC	homozygous	111023425
17	30709923	30709924	A	G	18	GENIC	homozygous	111023427
17	30711389	30711390	C	T	28	GENIC	homozygous	111023429
17	30712226	30712227	C	T	16	GENIC	homozygous	111023431