chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	155710071	155710072	C	T	55	GENIC	possibly homozygous	112896682
4	155710212	155710213	A	G	46	GENIC	homozygous	112896684
4	155711069	155711070	C	T	54	GENIC	homozygous	112896686
4	155711078	155711079	C	A	54	GENIC	homozygous	112896688
4	155711245	155711246	C	T	56	GENIC	homozygous	112896690
4	155711392	155711393	A	G	55	GENIC	homozygous	112896692
4	155711489	155711490	A	G	50	GENIC	homozygous	112896694
4	155712838	155712840	AT		60	GENIC	homozygous	128094685
4	155713205	155713206	T	G	38	GENIC	homozygous	112896696
4	155714892	155714893	C	T	48	GENIC	homozygous	112896698
4	155715142	155715143	C	G	19	GENIC	homozygous	112896700
4	155715419	155715420	C	T	44	GENIC	homozygous	112896702
4	155717462	155717463	G	A	53	GENIC	homozygous	112896704
4	155718142	155718142		TTA	47	GENIC	homozygous	128094686
4	155718928	155718929	C	A	51	GENIC	homozygous	112896706
4	155719390	155719391	A	C	43	GENIC	homozygous	119282346
4	155719431	155719432	C	T	43	GENIC	homozygous	112896708
4	155719868	155719869	G	A	53	GENIC	homozygous	112896710
4	155719916	155719917	C	G	55	GENIC	homozygous	112896712
4	155720563	155720564	A	G	38	GENIC	homozygous	112896714
4	155720688	155720689	T	C	33	GENIC	homozygous	112896716