chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	56595905	56595906	A	T	16	GENIC	homozygous	51892541
10	56595991	56595992	C	A	5	GENIC	homozygous	52059414
10	56596305	56596306	G	A	11	GENIC	possibly homozygous	51892544
10	56596322	56596323	T	C	7	GENIC	homozygous	51892547
10	56596472	56596473	G	C	28	GENIC	possibly homozygous	51892550
10	56596763	56596764	G	A	23	GENIC	homozygous	51892553
10	56597189	56597190	T	G	17	GENIC	homozygous	51656163
10	56597336	56597337	T	G	14	GENIC	homozygous	51656165
10	56597367	56597368	T	C	11	GENIC	heterozygous	51892559
10	56597405	56597406	G	A	13	GENIC	possibly homozygous	51892562
10	56597665	56597666	T	-	5	GENIC	homozygous	51892568
10	56598312	56598313	G	A	11	GENIC	homozygous	51892571
10	56599144	56599145	A	T	16	GENIC	homozygous	51892574
10	56599371	56599372	A	G	15	GENIC	homozygous	51892577
10	56599841	56599842	G	C	14	GENIC	possibly homozygous	51892580
10	56600132	56600133	A	G	11	GENIC	possibly homozygous	51656171
10	56600367	56600368	G	A	17	GENIC	possibly homozygous	51892583
10	56600797	56600798	T	C	15	GENIC	possibly homozygous	51892586
10	56601118	56601119	A	G	15	GENIC	homozygous	51892595
10	56601492	56601493	T	G	16	GENIC	homozygous	51892601
10	56601745	56601746	A	G	12	GENIC	homozygous	51656181
10	56601971	56601972	G	A	24	GENIC	possibly homozygous	52059416
10	56602632	56602633	A	G	25	GENIC	possibly homozygous	51656183
10	56602978	56602979	C	T	16	GENIC	possibly homozygous	51892604
10	56603744	56603745	T	C	13	GENIC	homozygous	51656185
10	56604501	56604502	C	T	22	GENIC	homozygous	51892607
10	56606422	56606423	T	A	24	GENIC	possibly homozygous	51656189
10	56607240	56607241	C	-	2	GENIC	heterozygous	51892613
10	56607364	56607365	A	G	9	GENIC	heterozygous	51656193
10	56607711	56607712	T	C	20	GENIC	possibly homozygous	52059418
10	56607742	56607743	A	G	14	GENIC	possibly homozygous	51656195
10	56607749	56607750	C	T	11	GENIC	homozygous	52059420