chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	109529732	109529733	A	G	7	GENIC	homozygous	113373217
4	109529949	109529950	T	A	19	GENIC	homozygous	113373219
4	109530037	109530038	C	T	20	GENIC	homozygous	119403639
4	109530038	109530039	T	C	20	GENIC	homozygous	119403640
4	109530455	109530456	T	C	23	GENIC	homozygous	113373221
4	109530617	109530618	G	C	14	GENIC	homozygous	113373223
4	109531091	109531092	G	C	15	GENIC	homozygous	113373229
4	109531271	109531272	A	G	20	GENIC	homozygous	113373231
4	109531448	109531449	C	T	25	GENIC	homozygous	113373235
4	109531567	109531568	C	A	11	GENIC	homozygous	113598113
4	109531641	109531642	C	A	14	GENIC	possibly homozygous	113373241
4	109531771	109531772	A	C	18	GENIC	homozygous	113373243
4	109531772	109531773	T	C	18	GENIC	homozygous	113373245
4	109531836	109531837	T	C	22	GENIC	homozygous	113373247
4	109532066	109532066		CTT	19	GENIC	homozygous	133130846
4	109532145	109532146	T	C	15	GENIC	homozygous	113373251