chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	172121462	172121463	A	G	69	GENIC	homozygous	112953409
4	172122519	172122520	G	A	51	GENIC	homozygous	113217537
4	172122639	172122655	CTATCTATCTACCTAC		27	GENIC	heterozygous	130940634
4	172124453	172124454	A	G	48	GENIC	homozygous	112953419
4	172128819	172128820	A	G	53	GENIC	homozygous	112953423
4	172129011	172129012	C	T	22	GENIC	homozygous	113564120
4	172125995	172125999	TCTT		33	GENIC	possibly homozygous	128105070
4	172124504	172124505	G	C	44	GENIC	homozygous	113564117
4	172124918	172124919	G	A	50	GENIC	homozygous	113564118
4	172129007	172129008	C	T	21	GENIC	homozygous	113564119
4	172129022	172129024	CC		22	GENIC	homozygous	130940635
4	172129277	172129278	T	C	45	GENIC	homozygous	113217559
4	172129608	172129609	C	T	56	GENIC	homozygous	113564121
4	172130402	172130403	A	G	53	GENIC	homozygous	113564122
4	172130602	172130603	A	G	70	GENIC	homozygous	112953425
4	172132125	172132126	A	G	61	GENIC	possibly homozygous	112953429
4	172132384	172132385	T	C	48	GENIC	homozygous	112953431
4	172132443	172132444	A	G	51	GENIC	homozygous	112953433
4	172132590	172132591	A	G	77	GENIC	possibly homozygous	112953435
4	172132812	172132813	T	G	55	GENIC	homozygous	112953437
4	172132975	172132976	G	A	50	GENIC	homozygous	113564123
4	172133196	172133206	TGTCTCTGTG		50	GENIC	homozygous	130940637
4	172133314	172133315	T	C	54	GENIC	homozygous	112953439
4	172133533	172133534	G	A	46	GENIC	homozygous	113067984
4	172133697	172133698	A	G	40	GENIC	homozygous	112953445
4	172133779	172133780	T	G	50	GENIC	homozygous	112953447
4	172133948	172133949	G	A	55	GENIC	homozygous	113217563
4	172133983	172133984	T	C	59	GENIC	homozygous	112953449
4	172134013	172134014	C	T	61	GENIC	possibly homozygous	113217564