chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	111834152	111834153	A	G	11	GENIC	homozygous	111674992
3	111834635	111834636	A	G	10	GENIC	homozygous	112005735
3	111835416	111835417	A	G	11	GENIC	homozygous	111674993
3	111835651	111835652	G	A	11	GENIC	homozygous	111674994
3	111836584	111836585	A	G	7	GENIC	homozygous	111674996
3	111836969	111836970	G	A	10	GENIC	homozygous	111674997
3	111837263	111837264	T	A	15	GENIC	homozygous	111674998
3	111837833	111837834	A	G	14	GENIC	homozygous	111675004
3	111841092	111841093	C	A	22	GENIC	homozygous	112005737
3	111841272	111841273	C	T	12	GENIC	homozygous	112005739
3	111846181	111846182	G	A	11	GENIC	homozygous	112005741
3	111849500	111849501	T	C	9	GENIC	homozygous	111675022
3	111854944	111854945	C	T	8	GENIC	homozygous	112005743
3	111856361	111856362	T	G	14	GENIC	homozygous	111675037
3	111858149	111858150	A	G	7	GENIC	homozygous	111675044
3	111859879	111859880	C	T	9	GENIC	homozygous	112005749
3	111860850	111860851	G	A	7	GENIC	possibly homozygous	112005751
3	111861043	111861044	C	T	14	GENIC	homozygous	112005753
3	111861332	111861333	C	A	11	GENIC	homozygous	112005755
3	111865538	111865539	G	T	16	GENIC	homozygous	111675061
3	111865704	111865705	C	T	10	GENIC	homozygous	112005757
3	111868118	111868119	A	G	6	GENIC	homozygous	111675066
3	111868941	111868942	G	T	17	GENIC	homozygous	112005759
3	111870142	111870143	T	C	9	GENIC	homozygous	111675070
3	111871172	111871173	C	T	7	GENIC	homozygous	112005761
3	111874793	111874794	G	A	16	GENIC	homozygous	112005763
3	111874948	111874949	C	T	10	GENIC	homozygous	112005765