chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	73512649	73512650	A	G	59	GENIC	homozygous	113860077
5	73513612	73513613	T	C	69	GENIC	homozygous	113860079
5	73513937	73513938	A	T	57	GENIC	homozygous	113860081
5	73515229	73515230	A	C	58	GENIC	homozygous	113860083
5	73515233	73515234	A	C	57	GENIC	heterozygous	113860085
5	73519318	73519319	A	G	74	GENIC	homozygous	113860089
5	73522158	73522159	C	A	56	GENIC	possibly homozygous	113860095
5	73523284	73523285	T	C	53	GENIC	homozygous	113860097
5	73523513	73523514	A	C	28	GENIC	homozygous	113860099
5	73528268	73528269	G	A	61	GENIC	homozygous	113860101
5	73528525	73528526	C	G	54	GENIC	homozygous	113860103
5	73528828	73528829	A	C	63	GENIC	homozygous	113860105
5	73529221	73529222	T	G	53	GENIC	homozygous	113860107
5	73529255	73529256	T	G	44	GENIC	possibly homozygous	113860109
5	73529478	73529479	C	T	64	GENIC	homozygous	113860111
5	73529721	73529722	G	A	51	GENIC	homozygous	113860113
5	73529840	73529841	G	A	47	GENIC	heterozygous	113860115
5	73529851	73529852	G	A	43	GENIC	heterozygous	113860117
5	73529861	73529862	A	G	44	GENIC	possibly homozygous	113860119
5	73529870	73529871	A	G	46	GENIC	homozygous	113860121
5	73529936	73529937	A	G	63	GENIC	homozygous	113860123
5	73530338	73530339	A	C	47	GENIC	homozygous	113860125
5	73530658	73530659	T	C	54	GENIC	possibly homozygous	113860127
5	73531318	73531319	A	G	50	GENIC	homozygous	113860129
5	73534834	73534835	A	G	43	GENIC	homozygous	113860131
5	73535287	73535288	C	T	46	GENIC	possibly homozygous	113860133
5	73529824	73529825	A	G	48	GENIC	heterozygous	114125945
5	73540152	73540153	G	T	23	GENIC	homozygous	113860135
5	73546762	73546763	A	G	20	GENIC	possibly homozygous	113860137
5	73551099	73551100	A	G	52	GENIC	homozygous	113860139