chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	226976664	226976664		G	23	GENIC	homozygous	131782988
1	226976832	226976833	C	T	42	GENIC	homozygous	108998577
1	226977270	226977271	G	A	47	GENIC	homozygous	108998578
1	226977389	226977390	T	C	44	GENIC	homozygous	108998579
1	226979733	226979734	C	T	35	GENIC	homozygous	108998580
1	226981679	226981680	G	A	48	GENIC	homozygous	108998581
1	226982031	226982032	C	T	38	GENIC	homozygous	108998582
1	226983197	226983198	G	A	49	GENIC	homozygous	108998583
1	226984410	226984411	G	A	41	GENIC	homozygous	108998584
1	226984929	226984929		TTC	40	GENIC	homozygous	131263751
1	226986081	226986082	G	C	46	GENIC	homozygous	108998589
1	226986289	226986290	C	T	45	GENIC	homozygous	108998590
1	226987423	226987424	A	G	46	GENIC	homozygous	108998593
1	226986463	226986464	T	C	56	GENIC	homozygous	108998591
1	226986533	226986534	A	G	37	GENIC	homozygous	108998592
1	226977510	226977514	AAAC		41	GENIC	homozygous	132539161
1	226981497	226981498	A		32	GENIC	homozygous	132539162
1	226987756	226987757	T	C	71	GENIC	homozygous	108998594
1	226988554	226988555	T	C	30	GENIC	possibly homozygous	108998595
1	226988622	226988623	C	G	42	GENIC	homozygous	108998596
1	226988701	226988731	TGTGTGTGAGTGCGTGTGTTTGAGTGTGTA		39	GENIC	possibly homozygous	132539163
1	226989829	226989829		AC	38	GENIC	homozygous	131782991
1	226990504	226990505	C	T	45	GENIC	homozygous	108998597
1	226991161	226991162	G	A	50	GENIC	homozygous	108998598
1	226991290	226991291	T	C	48	GENIC	homozygous	108998599
1	226992745	226992746	T	A	38	GENIC	homozygous	108998600
1	226990802	226990803	A	G	52	GENIC	homozygous	120490665