chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	172155124	172155125	G	A	26	GENIC	homozygous	112208826
3	172155936	172155936		G	10	GENIC	homozygous	130915659
3	172161719	172161720	C	T	16	GENIC	possibly homozygous	112208834
3	172164091	172164092	T	C	19	GENIC	homozygous	112208895
3	172165407	172165408	G	A	17	GENIC	homozygous	112208896
3	172166338	172166339	A	G	28	GENIC	homozygous	112208898
3	172167823	172167824	T	C	25	GENIC	homozygous	112208900
3	172169406	172169407	T	A	18	GENIC	homozygous	112208902
3	172170423	172170424	C	T	14	GENIC	homozygous	112208904
3	172170661	172170662	C	T	18	GENIC	possibly homozygous	112208906
3	172171300	172171301	G	A	42	GENIC	heterozygous	130545339
3	172173674	172173674		TAT	17	GENIC	homozygous	130915660
3	172175277	172175278	G	A	21	GENIC	homozygous	112208914
3	172173008	172173009	C	T	14	GENIC	heterozygous	121923405
3	172173029	172173030	T	C	12	GENIC	heterozygous	121923406
3	172173680	172173681	C	T	15	GENIC	homozygous	112208910
3	172174626	172174627	G	C	25	GENIC	homozygous	112208912
3	172171129	172171130	C	T	26	GENIC	heterozygous	130292639
3	172171831	172171832	A	G	29	GENIC	heterozygous	131844836
3	172172002	172172003	T	A	16	GENIC	heterozygous	135306990
3	172172358	172172359	G	A	26	GENIC	heterozygous	135306991
3	172176129	172176130	C	A	24	GENIC	homozygous	112208916
3	172176191	172176192	C		22	GENIC	homozygous	127961987
3	172176206	172176207	G		21	GENIC	homozygous	127961988
3	172176226	172176228	CC		20	GENIC	homozygous	127961989
3	172176232	172176234	CC		18	GENIC	homozygous	127961990
3	172177645	172177646	A	G	18	GENIC	homozygous	112208918
3	172177723	172177724	A	C	12	GENIC	homozygous	112208920
3	172178320	172178320		T	20	GENIC	possibly homozygous	130915661
3	172181094	172181095	T	C	18	GENIC	homozygous	112208922
3	172181199	172181200	G	A	23	GENIC	homozygous	112208924
3	172181313	172181314	A	G	21	GENIC	homozygous	112208926
3	172183214	172183214		G	26	GENIC	homozygous	130915662