chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10657477	10657478	T	A	37	GENIC	homozygous	117804000
9	10665372	10665373	T	C	33	GENIC	homozygous	117804001
9	10665626	10665627	G	T	29	GENIC	homozygous	117804002
9	10667394	10667395	A	G	25	GENIC	homozygous	117804003
9	10667563	10667564	C	T	26	GENIC	homozygous	117804004
9	10669642	10669643	T	C	43	GENIC	homozygous	117804005
9	10671257	10671258	G	A	35	GENIC	homozygous	117804006
9	10672068	10672069	T	C	41	GENIC	homozygous	117804007
9	10674515	10674516	A	G	26	GENIC	homozygous	117804008
9	10683046	10683047	G	T	35	GENIC	homozygous	117804009
9	10683349	10683350	T	C	21	GENIC	homozygous	117804010
9	10686456	10686457	T	C	29	GENIC	homozygous	117804011
9	10686954	10686955	C	G	38	GENIC	homozygous	117804012
9	10692330	10692331	A	G	28	GENIC	homozygous	117804013
9	10695017	10695018	C	T	26	GENIC	homozygous	117804014
9	10696134	10696135	A	G	38	GENIC	homozygous	117804015
9	10699827	10699828	T	A	36	GENIC	homozygous	117804016
9	10702849	10702850	A	G	41	GENIC	homozygous	117244404
9	10709713	10709714	A	T	20	GENIC	homozygous	117676013
9	10709714	10709715	C	A	21	GENIC	homozygous	117764068
9	10711131	10711132	A	G	35	GENIC	homozygous	117804017
9	10716926	10716927	G	A	38	GENIC	homozygous	117804018
9	10727413	10727414	C	T	19	GENIC	homozygous	117804019
9	10731033	10731034	A	G	38	GENIC	homozygous	117804020
9	10731196	10731197	A	G	30	GENIC	homozygous	117804021