chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	57674100	57674101	A	G	11	GENIC	homozygous	56908837
4	57674868	57674869	C	T	2	GENIC	homozygous	57730741
4	57675277	57675278	G	C	14	GENIC	possibly homozygous	57730743
4	57675774	57675775	C	T	16	GENIC	homozygous	57730745
4	57675893	57675894	T	C	9	GENIC	homozygous	57730747
4	57675976	57675977	T	A	10	GENIC	possibly homozygous	57730749
4	57676550	57676551	G	A	7	GENIC	homozygous	57730753
4	57676558	57676559	G	C	11	GENIC	possibly homozygous	57730755
4	57676638	57676639	G	A	13	GENIC	homozygous	57730757
4	57676826	57676827	A	G	15	GENIC	homozygous	57730759
4	57677665	57677666	T	TAA	5	GENIC	heterozygous	57730763
4	57677665	57677666	T	TA	5	GENIC	heterozygous	57834969
4	57677730	57677731	G	A	5	GENIC	homozygous	57730765
4	57678171	57678172	C	T	16	GENIC	homozygous	57730767
4	57680000	57680001	C	T	8	GENIC	possibly homozygous	57730771
4	57680197	57680198	A	G	11	GENIC	possibly homozygous	56908839
4	57680502	57680503	T	A	11	GENIC	homozygous	57730773
4	57681491	57681492	A	G	7	GENIC	homozygous	57730775
4	57681934	57681943	TCCTCCTCT	---------	4	GENIC	heterozygous	57730777
4	57681969	57681970	C	T	2	GENIC	homozygous	57730791
4	57681975	57681976	A	T	2	GENIC	homozygous	57730793
4	57682319	57682320	G	A	11	GENIC	homozygous	57730795
4	57683199	57683200	C	A	7	GENIC	homozygous	57730797
4	57683868	57683873	ATGTT	-----	2	GENIC	homozygous	57730799
4	57684064	57684065	C	G	16	GENIC	homozygous	57730801
4	57684645	57684646	C	T	24	GENIC	homozygous	56908842
4	57684791	57684792	A	G	11	GENIC	homozygous	56908843
4	57685337	57685338	G	C	15	GENIC	possibly homozygous	57730803
4	57685690	57685691	C	T	10	GENIC	homozygous	56908844
4	57685750	57685751	T	C	7	GENIC	possibly homozygous	56908845
4	57685755	57685756	T	C	6	GENIC	homozygous	56908846
4	57685830	57685831	T	C	6	GENIC	homozygous	57322122
4	57685831	57685832	A	T	5	GENIC	homozygous	56908847