chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479561	42479562	A	T	29	GENIC	possibly homozygous	50209153
12	42479566	42479567	T	G	29	GENIC	homozygous	50209154
12	42479572	42479573	T	C	30	GENIC	homozygous	50209155
12	42480660	42480661	C	CCA	10	GENIC	homozygous	50209156
12	42480940	42480941	C	T	22	GENIC	homozygous	50468947
12	42483951	42483952	G	-	39	GENIC	homozygous	50209157
12	42483952	42483953	G	GT	19	GENIC	heterozygous	50209158
12	42483953	42483954	T	-	19	GENIC	heterozygous	50209159
12	42483971	42483972	C	-	37	GENIC	heterozygous	50209160
12	42484707	42484708	C	T	38	GENIC	possibly homozygous	50209161
12	42484988	42484994	GTGTGT	------	7	GENIC	heterozygous	50209162
12	42485831	42485832	A	G	20	GENIC	homozygous	50209163
12	42486128	42486129	A	G	15	INTERGENIC	homozygous	50209164
12	42486270	42486271	A	AC	1	INTERGENIC	homozygous	50209165
12	42487665	42487666	A	C	24	GENIC	homozygous	50209167
12	42487706	42487707	C	T	26	GENIC	possibly homozygous	50209168
12	42487729	42487730	T	C	32	GENIC	homozygous	50209169
12	42488113	42488114	A	ATTT	5	GENIC	heterozygous	50209170
12	42488406	42488407	T	TTC	19	GENIC	possibly homozygous	50209171
12	42488411	42488421	TTTTTTTTAA	----------	14	GENIC	homozygous	50209172
12	42488412	42488421	TTTTTTTAA	---------	14	GENIC	possibly homozygous	50209173
12	42483952	42483953	G	T	46	GENIC	heterozygous	50486460
12	42488972	42488973	G	A	54	GENIC	homozygous	50209174
12	42490347	42490348	T	A	71	GENIC	homozygous	50209175
12	42490538	42490539	A	G	40	GENIC	homozygous	50209176
12	42490600	42490603	CGC	---	18	GENIC	possibly homozygous	50209177
12	42490601	42490602	G	-	18	GENIC	possibly homozygous	50209178
12	42490602	42490603	C	CACACACACA	4	GENIC	homozygous	50209179
12	42490657	42490658	C	T	34	GENIC	homozygous	50209180
12	42491393	42491394	C	T	32	GENIC	homozygous	50209181
12	42491647	42491648	C	T	9	GENIC	homozygous	50209182
12	42494101	42494102	C	A	42	INTERGENIC	homozygous	50209183
12	42494157	42494158	A	G	51	INTERGENIC	homozygous	50209184