chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	60421043	60421044	A	T	12	GENIC	homozygous	109778906
2	60421562	60421563	C	G	13	GENIC	homozygous	109778910
2	60421582	60421583	G	C	11	GENIC	homozygous	109778912
2	60421817	60421818	A	G	10	GENIC	heterozygous	109778914
2	60421892	60421893	C	A	15	GENIC	heterozygous	109778918
2	60421913	60421914	G	C	18	GENIC	heterozygous	109778920
2	60421999	60422000	G	A	24	GENIC	heterozygous	109778924
2	60422014	60422015	C	T	24	GENIC	homozygous	109778928
2	60422242	60422243	G	T	11	GENIC	heterozygous	110538203
2	60422449	60422450	G	A	14	GENIC	possibly homozygous	127790637
2	60422763	60422764	T	A	11	GENIC	possibly homozygous	132026230
2	60422793	60422794	G	A	12	GENIC	homozygous	127790640
2	60422861	60422862	G	A	12	GENIC	heterozygous	133382796
2	60423591	60423592	T	C	14	GENIC	possibly homozygous	109778930
2	60423942	60423943	A	C	10	GENIC	homozygous	132026231
2	60424497	60424498	T	C	3	GENIC	homozygous	127790646
2	60426631	60426632	T	A	9	GENIC	possibly homozygous	109778934
2	60427290	60427291	C	G	11	GENIC	heterozygous	127790650
2	60427513	60427514	A	G	12	GENIC	homozygous	110538221
2	60428051	60428052	A	C	21	GENIC	homozygous	109778936
2	60432339	60432340	G	T	17	GENIC	homozygous	120168499
2	60433314	60433315	A	T	28	GENIC	possibly homozygous	120168500
2	60433777	60433778	C	G	17	GENIC	homozygous	120168501
2	60433812	60433813	C	T	15	GENIC	homozygous	120168502
2	60436621	60436622	G	A	17	GENIC	possibly homozygous	120168503
2	60441372	60441373	C	T	20	GENIC	homozygous	120168504
2	60444587	60444588	C	T	16	GENIC	homozygous	120168505
2	60442060	60442061	T		17	GENIC	homozygous	127627235
2	60438096	60438096		ACATAGTAGGTAAAGAA	15	GENIC	homozygous	132013439
2	60427968	60427969	A		15	GENIC	homozygous	127627232