chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	1561227	1561228	G	A	56	GENIC	homozygous	139061199
12	1562350	1562351	T	C	65	GENIC	homozygous	139061201
12	1562471	1562472	T	G	61	GENIC	possibly homozygous	139061202
12	1565757	1565758	C	T	49	GENIC	homozygous	139061204
12	1566971	1566972	A	G	40	GENIC	homozygous	139061206
12	1568361	1568362	A	G	44	GENIC	homozygous	139061207
12	1569844	1569845	A	G	59	GENIC	homozygous	139061208
12	1570155	1570156	A	G	56	GENIC	homozygous	139061209
12	1571760	1571761	T	C	32	GENIC	homozygous	139061210
12	1572738	1572739	A	G	72	GENIC	homozygous	139061211
12	1572779	1572780	C	T	63	GENIC	homozygous	139061212
12	1571941	1571943	TG		25	GENIC	homozygous	139035654
12	1571978	1571994	TGTGTGTGTATGTGCC		25	GENIC	homozygous	139035655
12	1573367	1573368	A	T	50	GENIC	homozygous	139061213
12	1573368	1573369	T	C	49	GENIC	homozygous	139061214