chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24738473	24738474	C	T	35	GENIC	homozygous	50136134
12	24738824	24738825	G	A	31	GENIC	homozygous	50136136
12	24738938	24738939	T	A	25	GENIC	homozygous	50136138
12	24738968	24738969	G	C	25	GENIC	homozygous	50136140
12	24739103	24739104	T	-	19	GENIC	heterozygous	50136144
12	24739367	24739368	C	CG	42	GENIC	homozygous	50136146
12	24739504	24739505	C	T	39	GENIC	homozygous	50136148
12	24739691	24739692	C	T	32	GENIC	homozygous	50136150
12	24739787	24739788	G	A	36	GENIC	homozygous	50136152
12	24739853	24739854	A	-	18	GENIC	heterozygous	50136154
12	24740533	24740534	T	A	33	GENIC	homozygous	50136156
12	24741627	24741628	G	A	28	GENIC	homozygous	50136158
12	24742023	24742024	A	AACAC	7	GENIC	possibly homozygous	50136160
12	24742062	24742063	C	CTTTTATTTTT	6	GENIC	homozygous	50136162
12	24742090	24742091	T	C	16	GENIC	homozygous	50136164
12	24743125	24743126	C	CGT	4	GENIC	homozygous	50136168
12	24744412	24744413	C	G	16	GENIC	heterozygous	50136170
12	24744426	24744427	C	G	13	GENIC	heterozygous	50136172
12	24744441	24744443	TC	--	8	GENIC	possibly homozygous	50293789