chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	143820874	143820874		TTTG	31	GENIC	homozygous	128531494
7	143823278	143823280	AG		29	GENIC	homozygous	128531495
7	143823581	143823581		G	27	GENIC	homozygous	128531496
7	143823699	143823700	A	G	39	GENIC	homozygous	115944685
7	143825659	143825659		T	24	GENIC	possibly homozygous	128531497
7	143826120	143826121	G	T	48	GENIC	homozygous	115944687
7	143826140	143826141	C	T	52	GENIC	homozygous	116100799
7	143826854	143826855	G	A	48	GENIC	homozygous	115944688
7	143827261	143827262	A	G	12	GENIC	homozygous	115944690
7	143827353	143827354	T	G	9	GENIC	heterozygous	132120719
7	143828599	143828600	G	A	35	GENIC	homozygous	115944691
7	143829200	143829201	G	A	45	GENIC	homozygous	115944692
7	143829430	143829431	A	G	33	GENIC	homozygous	116100801
7	143829503	143829504	G	A	35	GENIC	homozygous	116100803
7	143829736	143829737	A	G	45	GENIC	homozygous	115944693
7	143830114	143830115	T	C	43	GENIC	homozygous	115944701
7	143830394	143830394		AATAGTCGAGTCTGTTA	22	GENIC	homozygous	128531501
7	143830866	143830867	G	A	35	GENIC	homozygous	115944703
7	143835379	143835379		T	26	GENIC	heterozygous	128531502
7	143836445	143836446	C	T	36	GENIC	homozygous	116100811
7	143836849	143836850	G	A	43	GENIC	homozygous	116100813
7	143835849	143835850	G	A	13	GENIC	heterozygous	128564430
7	143829981	143829982	G		28	GENIC	homozygous	131026105