chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104053280	104053280		G	14	GENIC	homozygous	128855578
10	104053824	104053824		G	33	GENIC	homozygous	128855579
10	104053836	104053837	A		34	GENIC	homozygous	128855580
10	104053840	104053840		G	34	GENIC	homozygous	128855581
10	104053845	104053846	T	C	32	GENIC	homozygous	116713700
10	104054026	104054028	AG		1	GENIC	homozygous	128855595
10	104054034	104054035	G		1	GENIC	homozygous	128855596
10	104054035	104054036	G	T	1	GENIC	homozygous	123417428
10	104054044	104054045	T		1	GENIC	homozygous	128855597
10	104054050	104054051	G		1	GENIC	homozygous	128855598
10	104054054	104054055	G		1	GENIC	homozygous	128855599
10	104054068	104054069	T		1	GENIC	homozygous	128855600
10	104054072	104054072		CGCGC	1	GENIC	homozygous	128855601
10	104054075	104054076	G		1	GENIC	homozygous	128855602
10	104054088	104054088		C	1	GENIC	homozygous	128855603
10	104054101	104054102	A		1	GENIC	homozygous	128855604
10	104054598	104054599	G	C	5	GENIC	homozygous	129974159
10	104054602	104054602		G	5	GENIC	homozygous	128855605
10	104054607	104054607		C	5	GENIC	homozygous	128855606
10	104054609	104054609		A	5	GENIC	homozygous	128855607
10	104054622	104054622		C	7	GENIC	homozygous	128855608
10	104054626	104054627	G		8	GENIC	homozygous	128855609
10	104054632	104054632		C	8	GENIC	homozygous	128855610
10	104054636	104054636		C	10	GENIC	homozygous	128855611
10	104054644	104054644		G	12	GENIC	homozygous	128855612
10	104054656	104054657	G		13	GENIC	homozygous	128855613
10	104054663	104054664	G	T	12	GENIC	homozygous	117297447
10	104054667	104054668	G		13	GENIC	homozygous	128855614
10	104054682	104054683	G		15	GENIC	homozygous	128855615
10	104054688	104054689	T	C	15	GENIC	homozygous	117297449
10	104054697	104054697		G	17	GENIC	homozygous	128855616
10	104054701	104054701		G	18	GENIC	homozygous	128855617
10	104054600	104054600		G	5	GENIC	homozygous	129970934