chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42479561	42479562	A	T	18	GENIC	homozygous	50209153
12	42479566	42479567	T	G	21	GENIC	homozygous	50209154
12	42479572	42479573	T	C	22	GENIC	homozygous	50209155
12	42480660	42480661	C	CCACA	6	GENIC	homozygous	50544348
12	42483114	42483157	AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC	-------------------------------------------	17	GENIC	heterozygous	50544349
12	42483951	42483952	G	-	16	GENIC	heterozygous	50209157
12	42483952	42483954	GT	--	19	GENIC	heterozygous	50559071
12	42484707	42484708	C	T	29	GENIC	homozygous	50209161
12	42487665	42487666	A	C	27	GENIC	homozygous	50209167
12	42487706	42487707	C	T	22	GENIC	homozygous	50209168
12	42487729	42487730	T	C	21	GENIC	homozygous	50209169
12	42488113	42488114	A	ATTTTT	9	GENIC	heterozygous	50544352
12	42488412	42488421	TTTTTTTAA	---------	11	GENIC	possibly homozygous	50209173
12	42488972	42488973	G	A	34	GENIC	homozygous	50209174
12	42490347	42490348	T	A	31	GENIC	homozygous	50209175
12	42490538	42490539	A	G	21	GENIC	homozygous	50209176
12	42490601	42490602	G	A	4	GENIC	homozygous	50544353
12	42490602	42490603	C	CACACACACA	4	GENIC	heterozygous	50209179
12	42490602	42490603	C	CACACACA	4	GENIC	heterozygous	50544354
12	42490657	42490658	C	T	17	GENIC	homozygous	50209180
12	42491393	42491394	C	T	20	GENIC	homozygous	50209181
12	42494101	42494102	C	A	43	INTERGENIC	homozygous	50209183
12	42494157	42494158	A	G	32	INTERGENIC	homozygous	50209184