chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	166999479	166999480	T	C	18	GENIC	homozygous	108357376
1	167000311	167000312	A	G	36	GENIC	homozygous	108357378
1	167000479	167000480	G	A	36	GENIC	homozygous	108357379
1	167001076	167001077	C	T	28	GENIC	homozygous	108357380
1	167002104	167002105	G	C	20	GENIC	homozygous	108357381
1	167002745	167002746	T	A	18	GENIC	homozygous	108357382
1	167003507	167003508	T	C	21	GENIC	homozygous	108357383
1	167007763	167007764	A	C	24	GENIC	homozygous	108357389
1	167009316	167009317	C	T	26	GENIC	homozygous	108357390
1	167009532	167009533	T	C	25	GENIC	homozygous	108357391
1	167009857	167009858	T	C	18	GENIC	homozygous	108357392
1	167010011	167010012	G	A	20	GENIC	homozygous	108357393
1	167010017	167010018	A	G	21	GENIC	homozygous	108357394
1	167011313	167011314	A	G	32	GENIC	homozygous	108357396
1	167011419	167011420	A	G	15	GENIC	homozygous	108357397
1	167011457	167011458	A	G	11	GENIC	homozygous	108357398
1	167011955	167011956	T	G	17	GENIC	homozygous	108357399
1	167013183	167013184	C	T	13	GENIC	homozygous	108357400
1	167013631	167013632	G	A	17	GENIC	homozygous	108357401
1	167014379	167014380	A	C	34	GENIC	homozygous	108357402
1	167014491	167014492	C	T	32	GENIC	homozygous	108357403
1	167014574	167014575	C	A	31	GENIC	homozygous	108357404