chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	129467972	129467973	G	A	29	GENIC	homozygous	52889531
8	129469874	129469875	G	-	2	GENIC	homozygous	53552280
8	129469876	129469883	AAGAAAG	-------	2	GENIC	homozygous	53552281
8	129471464	129471465	G	A	28	GENIC	homozygous	52889533
8	129471515	129471516	G	A	34	GENIC	homozygous	52889534
8	129471537	129471538	G	A	33	GENIC	homozygous	52889535
8	129471563	129471564	T	TC	28	GENIC	homozygous	52889536
8	129471627	129471628	T	C	34	GENIC	homozygous	52889537
8	129471701	129471702	G	A	26	GENIC	homozygous	52889538
8	129472470	129472471	T	TACAC	8	GENIC	possibly homozygous	52889540
8	129476893	129476894	A	T	26	GENIC	homozygous	52889541
8	129479799	129479801	AC	--	8	GENIC	heterozygous	53455996
8	129479875	129479876	A	AAC	10	GENIC	heterozygous	52889542
8	129480359	129480367	GAGAGAGA	--------	6	GENIC	heterozygous	53415617
8	129480721	129480722	C	G	31	GENIC	homozygous	52889544
8	129480734	129480735	C	G	32	GENIC	homozygous	52889545
8	129480745	129480746	T	C	33	GENIC	homozygous	52889546
8	129480758	129480759	T	G	32	GENIC	homozygous	52889547
8	129480786	129480787	G	-	34	GENIC	homozygous	52889548
8	129480793	129480794	A	C	32	GENIC	homozygous	52889549
8	129480799	129480800	A	-	33	GENIC	homozygous	52889550
8	129481241	129481242	A	-	1	GENIC	homozygous	53415618
8	129481514	129481515	C	T	41	GENIC	homozygous	52889551
8	129482363	129482364	C	T	41	GENIC	homozygous	52889552
8	129486724	129486725	G	A	34	GENIC	homozygous	52889553
8	129487861	129487862	C	CA	27	GENIC	possibly homozygous	52889554
8	129494676	129494677	A	G	27	GENIC	homozygous	52889555
8	129494881	129494882	C	T	36	GENIC	homozygous	52889556
8	129494973	129494974	G	A	26	GENIC	possibly homozygous	52889557
8	129495168	129495169	T	TC	7	GENIC	heterozygous	52889558
8	129495930	129495931	G	A	37	GENIC	possibly homozygous	52889559
8	129480788	129480789	G	A	33	GENIC	homozygous	53369680