chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	11146654	11146655	T	C	28	GENIC	possibly homozygous	116858841
10	11146662	11146663	T	C	27	GENIC	homozygous	116858843
10	11147101	11147102	A	G	45	GENIC	possibly homozygous	117074829
10	11147766	11147767	T	G	39	GENIC	homozygous	116734245
10	11147807	11147808	G	A	28	GENIC	homozygous	116858845
10	11147903	11147904	A	T	31	GENIC	homozygous	116858847
10	11147986	11147987	A	G	37	GENIC	homozygous	116734248
10	11148309	11148310	C	A	42	GENIC	homozygous	116494286
10	11148339	11148340	G	T	42	GENIC	homozygous	116734249
10	11148341	11148342	G	A	42	GENIC	homozygous	116734250
10	11148466	11148467	A	C	41	GENIC	homozygous	116734251
10	11148760	11148761	C	T	28	GENIC	homozygous	116734252
10	11148833	11148834	A	G	25	GENIC	possibly homozygous	116734253
10	11148862	11148863	G	T	19	GENIC	homozygous	116734254
10	11149117	11149118	A	G	36	GENIC	homozygous	116734255
10	11151092	11151093	T	A	34	GENIC	homozygous	117215720
10	11152401	11152402	A	G	41	GENIC	homozygous	116734256
10	11152965	11152966	A	G	28	GENIC	homozygous	116494290
10	11153482	11153483	C	T	34	GENIC	possibly homozygous	116734257
10	11153491	11153492	T	C	36	GENIC	homozygous	116734258
10	11153638	11153639	T	C	35	GENIC	homozygous	116734259
10	11153806	11153807	T	C	32	GENIC	homozygous	116734260