chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	10181377	10181378	G	T	4	GENIC	homozygous	111443866
3	10181562	10181563	A	G	15	GENIC	homozygous	111443867
3	10181880	10181881	T	A	23	GENIC	homozygous	111443868
3	10182047	10182048	T	C	15	GENIC	homozygous	111443869
3	10183694	10183695	C	T	26	GENIC	homozygous	111443872
3	10183888	10183889	C	T	23	GENIC	homozygous	111443873
3	10185512	10185513	T	G	4	GENIC	homozygous	111443875
3	10186348	10186349	G	A	28	GENIC	homozygous	111443878
3	10186802	10186803	T	C	16	GENIC	homozygous	111873843
3	10187203	10187204	A	G	17	GENIC	homozygous	111443880
3	10187667	10187668	C	T	11	GENIC	homozygous	111873845
3	10189343	10189344	C	T	22	GENIC	homozygous	111873849
3	10192860	10192861	T	C	24	GENIC	homozygous	111443883
3	10193420	10193421	T	C	18	GENIC	homozygous	111443884
3	10195961	10195962	C	T	17	GENIC	homozygous	111873851
3	10197536	10197537	C	T	21	GENIC	homozygous	111873853
3	10197666	10197667	C	T	18	GENIC	homozygous	111443887
3	10198904	10198905	T	A	13	GENIC	homozygous	111873855