chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	143138479	143138480	C	G	29	GENIC	homozygous	56961613
4	143138626	143138627	A	G	20	GENIC	homozygous	56961614
4	143138924	143138925	A	C	47	GENIC	possibly homozygous	56961616
4	143139182	143139183	A	G	35	GENIC	homozygous	56961617
4	143139263	143139264	T	A	48	GENIC	homozygous	56961618
4	143139823	143139824	C	T	28	GENIC	possibly homozygous	56961619
4	143140146	143140147	C	T	43	GENIC	homozygous	56961620
4	143140265	143140266	T	TC	34	GENIC	homozygous	56961621
4	143140485	143140486	G	GA	29	GENIC	possibly homozygous	56961622
4	143140853	143140854	A	G	32	GENIC	possibly homozygous	56961623
4	143142066	143142067	T	A	31	GENIC	homozygous	56961624
4	143142074	143142075	A	G	30	GENIC	homozygous	56961625
4	143142910	143142911	A	G	25	GENIC	possibly homozygous	56961626
4	143143094	143143095	T	A	22	GENIC	homozygous	56961628
4	143143272	143143294	CACACGCGCGCGCGCGCGCGCG	----------------------	5	GENIC	heterozygous	59496106
4	143144310	143144311	T	C	38	GENIC	homozygous	56961630
4	143144652	143144653	C	T	22	GENIC	homozygous	56961631
4	143144815	143144816	T	C	23	GENIC	homozygous	56961632
4	143145665	143145666	G	A	29	GENIC	homozygous	56961633
4	143145688	143145689	G	A	29	GENIC	homozygous	56961634
4	143145698	143145699	T	A	28	GENIC	homozygous	56961635
4	143146050	143146051	A	C	19	GENIC	homozygous	56961636