chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24738473	24738474	C	T	25	GENIC	homozygous	50136134
12	24738824	24738825	G	A	31	GENIC	homozygous	50136136
12	24738938	24738939	T	A	22	GENIC	homozygous	50136138
12	24738968	24738969	G	C	24	GENIC	homozygous	50136140
12	24739101	24739102	A	AT	14	GENIC	heterozygous	50538660
12	24739102	24739104	TT	--	14	GENIC	heterozygous	50136142
12	24739103	24739104	T	-	14	GENIC	heterozygous	50136144
12	24739367	24739368	C	CG	38	GENIC	homozygous	50136146
12	24739504	24739505	C	T	31	GENIC	homozygous	50136148
12	24739691	24739692	C	T	25	GENIC	homozygous	50136150
12	24739787	24739788	G	A	30	GENIC	homozygous	50136152
12	24739836	24739856	CACACACACACACACACACA	--------------------	17	GENIC	heterozygous	50538661
12	24739838	24739856	CACACACACACACACACA	------------------	17	GENIC	heterozygous	50538662
12	24740266	24740267	A	-	29	GENIC	heterozygous	50538663
12	24740533	24740534	T	A	31	GENIC	homozygous	50136156
12	24741627	24741628	G	A	23	GENIC	homozygous	50136158
12	24742023	24742024	A	AACAC	12	GENIC	heterozygous	50136160
12	24742023	24742024	A	AAC	12	GENIC	heterozygous	50538664
12	24742062	24742063	C	CTTTTATTTTT	19	GENIC	homozygous	50136162
12	24742090	24742091	T	C	23	GENIC	homozygous	50136164
12	24743125	24743126	C	CGT	3	GENIC	homozygous	50136168
12	24744398	24744406	CTCTCTCT	--------	9	GENIC	heterozygous	50538665